A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv706007



Internal ID15442659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:41322981..41323031hg38UCSC Ensembl
Innerchr6:41290719..41290769hg19UCSC Ensembl
Innerchr6:41398697..41398747hg18UCSC Ensembl
Innerchr6:41398697..41398747hg17UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3851
hg1951
hg1851
hg1751
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515617
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv706007
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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