A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526012



Internal ID15453305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:74372425..74375166hg38UCSC Ensembl
Innerchr3:74421576..74424317hg19UCSC Ensembl
Innerchr3:74504266..74507007hg18UCSC Ensembl
Innerchr3:74504266..74507007hg17UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg382742
hg192742
hg182742
hg172742
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702240
Samples
Known GenesCNTN3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526012
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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