A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526219



Internal ID15453512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:14657141..14663396hg38UCSC Ensembl
Innerchr9:14657139..14663394hg19UCSC Ensembl
Innerchr9:14647139..14653394hg18UCSC Ensembl
Innerchr9:14647139..14653394hg17UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg386256
hg196256
hg186256
hg176256
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702483
Samples
Known GenesZDHHC21
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526219
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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