A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521902



Internal ID15102509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:99331065..99337284hg38UCSC Ensembl
Innerchr13:99983319..99989538hg19UCSC Ensembl
Innerchr13:98781320..98787539hg18UCSC Ensembl
Innerchr13:98781320..98787539hg17UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg386220
hg196220
hg186220
hg176220
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694673
Samples
Known GenesMIR548AN, UBAC2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521902
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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