A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525773



Internal ID15453066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:75152482..75177477hg38UCSC Ensembl
Innerchr8:76064717..76089712hg19UCSC Ensembl
Innerchr8:76227272..76252267hg18UCSC Ensembl
Innerchr8:76227272..76252267hg17UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3824996
hg1924996
hg1824996
hg1724996
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701944
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525773
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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