A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668759



Internal ID15405411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:75210056..75278873hg38UCSC Ensembl
Innerchr2:75437182..75505999hg19UCSC Ensembl
Innerchr2:75290690..75359507hg18UCSC Ensembl
Innerchr2:75348837..75417654hg17UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3868818
hg1968818
hg1868818
hg1768818
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516509
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv668759
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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