A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156733



Internal ID15880350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:14639668..14662461hg38UCSC Ensembl
Innerchr9:14639666..14662459hg19UCSC Ensembl
Innerchr9:14629666..14652459hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3822794
hg1922794
hg1822794
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613643
Supporting Variants
SamplesNINDS_199
Known GenesZDHHC21
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156733
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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