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nsv5520945

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:792

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 151 SVs from 28 studies. See in: genome view    
Submitted genomic70,280,628-70,281,419Question Mark
Overlapping variant regions from other studies: 151 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):70,314,531-70,315,322Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5520945Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1670,280,62870,281,419
nsv5520945RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1670,314,53170,315,322

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17707191deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17707191Submitted genomicNC_000016.10:g.702
80628_70281419del
GRCh38 (hg38)NC_000016.10Chr1670,280,62870,281,419
nssv17707191RemappedPerfectNC_000016.9:g.7031
4531_70315322del
GRCh37.p13First PassNC_000016.9Chr1670,314,53170,315,322

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv17707191<0.00116404
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