A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589715



Internal ID16030438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:12813127..12976988hg38UCSC Ensembl
Innerchr3:12854626..13018488hg19UCSC Ensembl
Innerchr3:12829626..12993488hg18UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38163862
hg19163863
hg18163863
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151880
Samples1780862019_A
Known GenesCAND2, IQSEC1, RPL32, SNORA7A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589715
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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