A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584724



Internal ID16372133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:236752139..236811991hg38UCSC Ensembl
Innerchr2:237660782..237720634hg19UCSC Ensembl
Innerchr2:237325521..237385373hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3859853
hg1959853
hg1859853
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152349
SamplesHGDP01057
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584724
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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