A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527299



Internal ID15454592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113982908..114124520hg38UCSC Ensembl
Innerchr13:114752319..114889995hg19UCSC Ensembl
Innerchr13:113770421..113908097hg18UCSC Ensembl
Innerchr13:113770421..113908097hg17UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38141613
hg19137677
hg18137677
hg17137677
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv121n21
Supporting Variantsnssv703717
Samples
Known GenesRASA3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527299
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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