A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv666345



Internal ID15056311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:195624547..195656278hg38UCSC Ensembl
Innerchr2:196489271..196521002hg19UCSC Ensembl
Innerchr2:196197516..196229247hg18UCSC Ensembl
Innerchr2:196314777..196346508hg17UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg3831732
hg1931732
hg1831732
hg1731732
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515614
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv666345
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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