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nsv5461979

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,330

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 80 SVs from 11 studies. See in: genome view    
Submitted genomic72,188,493-72,190,822Question Mark
Overlapping variant regions from other studies: 80 SVs from 11 studies. See in: genome view    
Remapped(Score: Perfect):71,484,320-71,486,649Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5461979Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr572,188,49372,190,822
nsv5461979RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr571,484,32071,486,649

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16967503duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16967503Submitted genomicNC_000005.10:g.721
88493_72190822dup
GRCh38 (hg38)NC_000005.10Chr572,188,49372,190,822
nssv16967503RemappedPerfectNC_000005.9:g.7148
4320_71486649dup
GRCh37.p13First PassNC_000005.9Chr571,484,32071,486,649

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)
nssv16967503<0.00116404
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