A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525486



Internal ID15106093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2595063..2605773hg38UCSC Ensembl
Innerchr3:2636747..2647457hg19UCSC Ensembl
Innerchr3:2611747..2622457hg18UCSC Ensembl
Innerchr3:2611747..2622457hg17UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3810711
hg1910711
hg1810711
hg1710711
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701615
Samples
Known GenesCNTN4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525486
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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