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nsv6140741

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:64,001

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 444 SVs from 48 studies. See in: genome view    
Submitted genomic70,229,807-70,293,807Question Mark
Overlapping variant regions from other studies: 444 SVs from 48 studies. See in: genome view    
Remapped(Score: Perfect):69,525,634-69,589,634Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6140741Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr570,229,80770,293,807
nsv6140741RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr569,525,63469,589,634

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16967456deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16967456Submitted genomicNC_000005.10:g.702
29807_70293807del
GRCh38 (hg38)NC_000005.10Chr570,229,80770,293,807
nssv16967456RemappedPerfectNC_000005.9:g.6952
5634_69589634del
GRCh37.p13First PassNC_000005.9Chr569,525,63469,589,634

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)
nssv169674560.1546604278
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