A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519270



Internal ID15446563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:37467176..37471028hg38UCSC Ensembl
Innerchr13:38041313..38045165hg19UCSC Ensembl
Innerchr13:36939313..36943165hg18UCSC Ensembl
Innerchr13:36939313..36943165hg17UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg383853
hg193853
hg183853
hg173853
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv108n21
Supporting Variantsnssv655144, nssv661141
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519270
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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