A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152491



Internal ID15878659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:85604283..85640993hg38UCSC Ensembl
Innerchr3:85653433..85690143hg19UCSC Ensembl
Innerchr3:85736123..85772833hg18UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3836711
hg1936711
hg1836711
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590909
Supporting Variants
SamplesHGDP01238
Known GenesCADM2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152491
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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