A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525363



Internal ID15452656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:92835918..92842785hg38UCSC Ensembl
Innerchr9:95598200..95605067hg19UCSC Ensembl
Innerchr9:94638021..94644888hg18UCSC Ensembl
Innerchr9:92677755..92684622hg17UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg386868
hg196868
hg186868
hg176868
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701482
Samples
Known GenesANKRD19P
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525363
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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