A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152494



Internal ID15853283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:85868139..85957060hg38UCSC Ensembl
Innerchr3:85917289..86006210hg19UCSC Ensembl
Innerchr3:85999979..86088900hg18UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3888922
hg1988922
hg1888922
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590912
Supporting Variants
Samples1780854061_A
Known GenesCADM2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152494
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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