A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705161



Internal ID15441813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:127211236..127222770hg38UCSC Ensembl
Innerchr6:127532381..127543915hg19UCSC Ensembl
Innerchr6:127574074..127585608hg18UCSC Ensembl
Innerchr6:127574074..127585608hg17UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg3811535
hg1911535
hg1811535
hg1711535
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528549
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705161
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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