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nsv6140371

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:30,201

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 676 SVs from 52 studies. See in: genome view    
Submitted genomic70,949,800-70,980,000Question Mark
Overlapping variant regions from other studies: 676 SVs from 52 studies. See in: genome view    
Remapped(Score: Perfect):70,245,627-70,275,827Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6140371Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr570,949,80070,980,000
nsv6140371RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr570,245,62770,275,827

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16966821duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16966821Submitted genomicNC_000005.10:g.709
49800_70980000dup
GRCh38 (hg38)NC_000005.10Chr570,949,80070,980,000
nssv16966821RemappedPerfectNC_000005.9:g.7024
5627_70275827dup
GRCh37.p13First PassNC_000005.9Chr570,245,62770,275,827

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)
nssv169668210.014543824
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