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nsv6141054

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:24,001

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 726 SVs from 58 studies. See in: genome view    
Submitted genomic71,072,000-71,096,000Question Mark
Overlapping variant regions from other studies: 726 SVs from 58 studies. See in: genome view    
Remapped(Score: Perfect):70,367,827-70,391,827Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6141054Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr571,072,00071,096,000
nsv6141054RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr570,367,82770,391,827

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16966832duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16966832Submitted genomicNC_000005.10:g.710
72000_71096000dup
GRCh38 (hg38)NC_000005.10Chr571,072,00071,096,000
nssv16966832RemappedPerfectNC_000005.9:g.7036
7827_70391827dup
GRCh37.p13First PassNC_000005.9Chr570,367,82770,391,827

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)
nssv169668320.01272840
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