A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1128786



Internal ID15981972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:14592182..14639668hg38UCSC Ensembl
Innerchr9:14592180..14639666hg19UCSC Ensembl
Innerchr9:14582180..14629666hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3847487
hg1947487
hg1847487
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613642
Supporting Variants
Samples
Known GenesZDHHC21
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1128786
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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