A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613644



Internal ID16401053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:14662173..14689596hg38UCSC Ensembl
Innerchr9:14662171..14689594hg19UCSC Ensembl
Innerchr9:14652171..14679594hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3827424
hg1927424
hg1827424
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1128787
Samples
Known GenesZDHHC21
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613644
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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