A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699774



Internal ID15436426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:160814066..160839498hg38UCSC Ensembl
Innerchr6:161235098..161260530hg19UCSC Ensembl
Innerchr6:161155088..161180520hg18UCSC Ensembl
Innerchr6:161205509..161230941hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3825433
hg1925433
hg1825433
hg1725433
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523929
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699774
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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