A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589392



Internal ID16030115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2915430..2920170hg38UCSC Ensembl
Innerchr3:2957114..2961854hg19UCSC Ensembl
Innerchr3:2932114..2936854hg18UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg384741
hg194741
hg184741
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv957990
Samples
Known GenesCNTN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589392
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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