A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589376



Internal ID16030099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2329671..2363731hg38UCSC Ensembl
Innerchr3:2371355..2405415hg19UCSC Ensembl
Innerchr3:2346355..2380415hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3834061
hg1934061
hg1834061
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv957910
Samples
Known GenesCNTN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589376
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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