A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1139369



Internal ID15992555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:93168290..93215983hg38UCSC Ensembl
Innerchr9:95930572..95978265hg19UCSC Ensembl
Innerchr9:94970393..95018086hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3847694
hg1947694
hg1847694
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614880
Supporting Variants
Samples
Known GenesWNK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1139369
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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