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nsv4786168

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:190

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 139 SVs from 33 studies. See in: genome view    
Remapped(Score: Perfect):7,190,966-7,191,155Question Mark
Overlapping variant regions from other studies: 139 SVs from 33 studies. See in: genome view    
Submitted genomic7,094,285-7,094,474Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4786168RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000017.11Chr177,190,9667,191,155
nsv4786168Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000017.10Chr177,094,2857,094,474

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16297340alu deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16297340RemappedPerfectNC_000017.11:g.719
0966_7191155del
GRCh38.p12First PassNC_000017.11Chr177,190,9667,191,155
nssv16297340Submitted genomicNC_000017.10:g.709
4285_7094474del
GRCh37 (hg19)NC_000017.10Chr177,094,2857,094,474

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv162973400.0024116834
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