A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584093



Internal ID16371502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:194311489..194427146hg38UCSC Ensembl
Innerchr2:195176213..195291870hg19UCSC Ensembl
Innerchr2:194884458..195000115hg18UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg38115658
hg19115658
hg18115658
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7238n54
Supporting Variantsnssv1151121
Samples1798860114_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584093
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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