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nsv5470777

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:51

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 109 SVs from 24 studies. See in: genome view    
Submitted genomic179,680,424-179,680,474Question Mark
Overlapping variant regions from other studies: 109 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):179,107,425-179,107,475Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5470777Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5179,680,424179,680,474
nsv5470777RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5179,107,425179,107,475

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16979756deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16979756Submitted genomicNC_000005.10:g.179
680424_179680474de
l
GRCh38 (hg38)NC_000005.10Chr5179,680,424179,680,474
nssv16979756RemappedPerfectNC_000005.9:g.1791
07425_179107475del
GRCh37.p13First PassNC_000005.9Chr5179,107,425179,107,475

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)
nssv16979756<0.00116404
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