A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152443



Internal ID15529591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2385346..2386154hg38UCSC Ensembl
Innerchr3:2427030..2427838hg19UCSC Ensembl
Innerchr3:2402030..2402838hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38809
hg19809
hg18809
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589378
Supporting Variants
SamplesHGDP00814
Known GenesCNTN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152443
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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