A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522385



Internal ID15449678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:30817230..30817462hg38UCSC Ensembl
Innerchr3:30858722..30858954hg19UCSC Ensembl
Innerchr3:30833726..30833958hg18UCSC Ensembl
Innerchr3:30833726..30833958hg17UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg38233
hg19233
hg18233
hg17233
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695164
Samples
Known GenesGADL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522385
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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