A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524736



Internal ID15105343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:74837747..74852480hg38UCSC Ensembl
Innerchr8:75749982..75764715hg19UCSC Ensembl
Innerchr8:75912537..75927270hg18UCSC Ensembl
Innerchr8:75912537..75927270hg17UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3814734
hg1914734
hg1814734
hg1714734
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700727
Samples
Known GenesPI15
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524736
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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