A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589946



Internal ID16377355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:22558595..22823856hg38UCSC Ensembl
Innerchr3:22600086..22865347hg19UCSC Ensembl
Innerchr3:22575090..22840351hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38265262
hg19265262
hg18265262
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv960108
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589946
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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