A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523566



Internal ID15104173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:83719417..83956886hg38UCSC Ensembl
Innerchr3:83768568..84006037hg19UCSC Ensembl
Innerchr3:83851258..84088727hg18UCSC Ensembl
Innerchr3:83851258..84088727hg17UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg38237470
hg19237470
hg18237470
hg17237470
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699347
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523566
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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