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nsv4763943

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 325 SVs from 62 studies. See in: genome view    
Remapped(Score: Perfect):195,767,512-195,767,512Question Mark
Overlapping variant regions from other studies: 119 SVs from 34 studies. See in: genome view    
Remapped(Score: Perfect):138,009-138,009Question Mark
Overlapping variant regions from other studies: 99 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):27,224-27,224Question Mark
Overlapping variant regions from other studies: 98 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):27,224-27,224Question Mark
Overlapping variant regions from other studies: 98 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):27,224-27,224Question Mark
Overlapping variant regions from other studies: 100 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):27,620-27,620Question Mark
Overlapping variant regions from other studies: 121 SVs from 34 studies. See in: genome view    
Remapped(Score: Perfect):138,009-138,009Question Mark
Overlapping variant regions from other studies: 98 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):27,224-27,224Question Mark
Overlapping variant regions from other studies: 326 SVs from 62 studies. See in: genome view    
Submitted genomic195,494,383-195,494,383Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4763943RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3195,767,512195,767,512
nsv4763943RemappedPerfectGRCh38.p12ALT_REF_LOCI_5Second PassNT_187689.1Chr3|NT_18
7689.1		138,009138,009
nsv4763943RemappedPerfectGRCh38.p12ALT_REF_LOCI_7Second PassNT_187691.1Chr3|NT_18
7691.1		27,22427,224
nsv4763943RemappedPerfectGRCh38.p12ALT_REF_LOCI_6Second PassNT_187690.1Chr3|NT_18
7690.1		27,22427,224
nsv4763943RemappedPerfectGRCh38.p12ALT_REF_LOCI_4Second PassNT_187688.1Chr3|NT_18
7688.1		27,22427,224
nsv4763943RemappedPerfectGRCh38.p12ALT_REF_LOCI_3Second PassNT_187678.1Chr3|NT_18
7678.1		27,62027,620
nsv4763943RemappedPerfectGRCh38.p12ALT_REF_LOCI_1Second PassNT_187532.1Chr3|NT_18
7532.1		138,009138,009
nsv4763943RemappedPerfectGRCh38.p12ALT_REF_LOCI_2Second PassNT_187649.1Chr3|NT_18
7649.1		27,22427,224
nsv4763943Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3195,494,383195,494,383

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16291971insertionSequencingSplit read mapping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16291971RemappedPerfectNT_187688.1:g.2722
4_27225ins93		GRCh38.p12Second PassNT_187688.1Chr3|NT_18
7688.1		27,22427,224
nssv16291971RemappedPerfectNT_187690.1:g.2722
4_27225ins93		GRCh38.p12Second PassNT_187690.1Chr3|NT_18
7690.1		27,22427,224
nssv16291971RemappedPerfectNT_187691.1:g.2722
4_27225ins93		GRCh38.p12Second PassNT_187691.1Chr3|NT_18
7691.1		27,22427,224
nssv16291971RemappedPerfectNT_187678.1:g.2762
0_27621ins93		GRCh38.p12Second PassNT_187678.1Chr3|NT_18
7678.1		27,62027,620
nssv16291971RemappedPerfectNT_187689.1:g.1380
09_138010ins93		GRCh38.p12Second PassNT_187689.1Chr3|NT_18
7689.1		138,009138,009
nssv16291971RemappedPerfectNT_187649.1:g.2722
4_27225ins93		GRCh38.p12Second PassNT_187649.1Chr3|NT_18
7649.1		27,22427,224
nssv16291971RemappedPerfectNT_187532.1:g.1380
09_138010ins93		GRCh38.p12Second PassNT_187532.1Chr3|NT_18
7532.1		138,009138,009
nssv16291971RemappedPerfectNC_000003.12:g.195
767512_195767513in
s93		GRCh38.p12First PassNC_000003.12Chr3195,767,512195,767,512
nssv16291971Submitted genomicNC_000003.11:g.195
494383_195494384in
s93		GRCh37 (hg19)NC_000003.11Chr3195,494,383195,494,383

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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