A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv922087



Internal ID16216043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:154752875..154772998hg38UCSC Ensembl
Innerchr2:155609387..155629510hg19UCSC Ensembl
Innerchr2:155317633..155337756hg18UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg3820124
hg1920124
hg1820124
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv583426
Supporting Variants
Samples
Known GenesKCNJ3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv922087
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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