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nsv6147007

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,491

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 156 SVs from 39 studies. See in: genome view    
Submitted genomic22,167,435-22,175,925Question Mark
Overlapping variant regions from other studies: 156 SVs from 39 studies. See in: genome view    
Remapped(Score: Perfect):22,167,664-22,176,154Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6147007Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr622,167,43522,175,925
nsv6147007RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr622,167,66422,176,154

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16980773mobile element deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16980773Submitted genomicNC_000006.12:g.221
67435_22175925del
GRCh38 (hg38)NC_000006.12Chr622,167,43522,175,925
nssv16980773RemappedPerfectNC_000006.11:g.221
67664_22176154del
GRCh37.p13First PassNC_000006.11Chr622,167,66422,176,154

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)
nssv169807730.008546404
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