A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515849



Internal ID15442906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:110089850..110109174hg38UCSC Ensembl
Innerchr13:110742197..110761521hg19UCSC Ensembl
Innerchr13:109540198..109559522hg18UCSC Ensembl
Innerchr13:109540198..109559522hg17UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3819325
hg1919325
hg1819325
hg1719325
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv681276, nssv681213, nssv680613, nssv671868, nssv684798, nssv668304, nssv665009, nssv671104
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515849
Frequency
Sample Size2026
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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