A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524378



Internal ID15104985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2162081..2435164hg38UCSC Ensembl
Innerchr3:2203765..2476848hg19UCSC Ensembl
Innerchr3:2178765..2451848hg18UCSC Ensembl
Innerchr3:2178765..2451848hg17UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38273084
hg19273084
hg18273084
hg17273084
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700293
Samples
Known GenesCNTN4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524378
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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