A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526023



Internal ID15453316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:45907984..45915609hg38UCSC Ensembl
Innerchr13:46482119..46489744hg19UCSC Ensembl
Innerchr13:45380120..45387745hg18UCSC Ensembl
Innerchr13:45380120..45387745hg17UCSC Ensembl
Cytoband13q14.12
Allele length
AssemblyAllele length
hg387626
hg197626
hg187626
hg177626
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702253
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526023
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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