A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524139



Internal ID15451432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:50579339..50579596hg38UCSC Ensembl
Innerchr13:51153475..51153732hg19UCSC Ensembl
Innerchr13:50051476..50051733hg18UCSC Ensembl
Innerchr13:50051476..50051733hg17UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38258
hg19258
hg18258
hg17258
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700017
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524139
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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