A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152442



Internal ID15506624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2312351..2910530hg38UCSC Ensembl
Innerchr3:2354035..2952214hg19UCSC Ensembl
Innerchr3:2329035..2927214hg18UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg38598180
hg19598180
hg18598180
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589375
Supporting Variants
Samples1780854080_A
Known GenesCNTN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152442
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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