A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv583472



Internal ID16370881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:159064389..159185572hg38UCSC Ensembl
Innerchr2:159920901..160042083hg19UCSC Ensembl
Innerchr2:159629147..159750329hg18UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg38121184
hg19121183
hg18121183
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv922439
Samples
Known GenesTANC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv583472
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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