A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517476



Internal ID15444769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:37491309..37547423hg38UCSC Ensembl
Innerchr13:38065446..38121560hg19UCSC Ensembl
Innerchr13:36963446..37019560hg18UCSC Ensembl
Innerchr13:36963446..37019560hg17UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3856115
hg1956115
hg1856115
hg1756115
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv661873, nssv667061, nssv667143, nssv659190, nssv663336, nssv678142, nssv686487, nssv688169, nssv685038, nssv667973, nssv652167, nssv677270, nssv682396, nssv680079, nssv675882, nssv682485, nssv681370, nssv659219, nssv662138, nssv653093, nssv689198, nssv678184, nssv652134, nssv678787, nssv652195, nssv687720, nssv662999, nssv676047, nssv653356, nssv665167, nssv688904, nssv670369, nssv665220, nssv679110, nssv679853, nssv662314
Samples
Known GenesLINC00547
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517476
Frequency
Sample Size2026
Observed Gain0
Observed Loss36
Observed Complex0
Frequencyn/a


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