A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527651



Internal ID15108258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:30996876..30998948hg38UCSC Ensembl
Innerchr8:30854392..30856464hg19UCSC Ensembl
Innerchr8:30973934..30976006hg18UCSC Ensembl
Innerchr8:30973934..30976006hg17UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg382073
hg192073
hg182073
hg172073
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704122
Samples
Known GenesPURG
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527651
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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