A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590901



Internal ID16378310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:85144904..85253323hg38UCSC Ensembl
Innerchr3:85194054..85302473hg19UCSC Ensembl
Innerchr3:85276744..85385163hg18UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg38108420
hg19108420
hg18108420
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv967543, nssv1152490
SamplesHGDP00963
Known GenesCADM2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590901
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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