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nsv6147076

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,008

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 219 SVs from 42 studies. See in: genome view    
Submitted genomic82,125,272-82,133,279Question Mark
Overlapping variant regions from other studies: 219 SVs from 42 studies. See in: genome view    
Remapped(Score: Perfect):81,421,091-81,429,098Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6147076Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr582,125,27282,133,279
nsv6147076RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr581,421,09181,429,098

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16968595mobile element deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16968595Submitted genomicNC_000005.10:g.821
25272_82133279del
GRCh38 (hg38)NC_000005.10Chr582,125,27282,133,279
nssv16968595RemappedPerfectNC_000005.9:g.8142
1091_81429098del
GRCh37.p13First PassNC_000005.9Chr581,421,09181,429,098

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)
nssv16968595<0.00126404
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