A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522496



Internal ID15449789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:56163500..56172563hg38UCSC Ensembl
Innerchr3:56197528..56206591hg19UCSC Ensembl
Innerchr3:56172568..56181631hg18UCSC Ensembl
Innerchr3:56172568..56181631hg17UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg389064
hg199064
hg189064
hg179064
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705864
Samples
Known GenesERC2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522496
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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