A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv904641



Internal ID15851911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:32653075..32876841hg38UCSC Ensembl
Innerchr2:32878142..33101908hg19UCSC Ensembl
Innerchr2:32731646..32955412hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38223767
hg19223767
hg18223767
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv581284
Supporting Variants
Samples
Known GenesLINC00486, TTC27
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv904641
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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