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nsv4763461

  • 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: 316 SVs from 64 studies. See in: genome view    
Remapped(Score: Perfect):195,788,563-195,788,563Question Mark
Overlapping variant regions from other studies: 82 SVs from 32 studies. See in: genome view    
Remapped(Score: Perfect):158,397-158,397Question Mark
Overlapping variant regions from other studies: 60 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):6,173-6,173Question Mark
Overlapping variant regions from other studies: 61 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):6,173-6,173Question Mark
Overlapping variant regions from other studies: 60 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):6,173-6,173Question Mark
Overlapping variant regions from other studies: 61 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):6,173-6,173Question Mark
Overlapping variant regions from other studies: 84 SVs from 33 studies. See in: genome view    
Remapped(Score: Perfect):166,371-166,371Question Mark
Overlapping variant regions from other studies: 60 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):6,173-6,173Question Mark
Overlapping variant regions from other studies: 316 SVs from 64 studies. See in: genome view    
Submitted genomic195,515,434-195,515,434Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4763461RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3195,788,563195,788,563
nsv4763461RemappedPerfectGRCh38.p12ALT_REF_LOCI_5Second PassNT_187689.1Chr3|NT_18
7689.1		158,397158,397
nsv4763461RemappedPerfectGRCh38.p12ALT_REF_LOCI_4Second PassNT_187688.1Chr3|NT_18
7688.1		6,1736,173
nsv4763461RemappedPerfectGRCh38.p12ALT_REF_LOCI_3Second PassNT_187678.1Chr3|NT_18
7678.1		6,1736,173
nsv4763461RemappedPerfectGRCh38.p12ALT_REF_LOCI_6Second PassNT_187690.1Chr3|NT_18
7690.1		6,1736,173
nsv4763461RemappedPerfectGRCh38.p12ALT_REF_LOCI_7Second PassNT_187691.1Chr3|NT_18
7691.1		6,1736,173
nsv4763461RemappedPerfectGRCh38.p12ALT_REF_LOCI_1Second PassNT_187532.1Chr3|NT_18
7532.1		166,371166,371
nsv4763461RemappedPerfectGRCh38.p12ALT_REF_LOCI_2Second PassNT_187649.1Chr3|NT_18
7649.1		6,1736,173
nsv4763461Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3195,515,434195,515,434

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16273386insertionSequencingSplit read mapping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16273386RemappedPerfectNT_187678.1:g.6173
_6174ins52		GRCh38.p12Second PassNT_187678.1Chr3|NT_18
7678.1		6,1736,173
nssv16273386RemappedPerfectNT_187688.1:g.6173
_6174ins52		GRCh38.p12Second PassNT_187688.1Chr3|NT_18
7688.1		6,1736,173
nssv16273386RemappedPerfectNT_187690.1:g.6173
_6174ins52		GRCh38.p12Second PassNT_187690.1Chr3|NT_18
7690.1		6,1736,173
nssv16273386RemappedPerfectNT_187691.1:g.6173
_6174ins52		GRCh38.p12Second PassNT_187691.1Chr3|NT_18
7691.1		6,1736,173
nssv16273386RemappedPerfectNT_187689.1:g.1583
97_158398ins52		GRCh38.p12Second PassNT_187689.1Chr3|NT_18
7689.1		158,397158,397
nssv16273386RemappedPerfectNT_187649.1:g.6173
_6174ins52		GRCh38.p12Second PassNT_187649.1Chr3|NT_18
7649.1		6,1736,173
nssv16273386RemappedPerfectNT_187532.1:g.1663
71_166372ins52		GRCh38.p12Second PassNT_187532.1Chr3|NT_18
7532.1		166,371166,371
nssv16273386RemappedPerfectNC_000003.12:g.195
788563_195788564in
s52		GRCh38.p12First PassNC_000003.12Chr3195,788,563195,788,563
nssv16273386Submitted genomicNC_000003.11:g.195
515434_195515435in
s52		GRCh37 (hg19)NC_000003.11Chr3195,515,434195,515,434

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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