A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524898



Internal ID15452191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:34635383..34645641hg38UCSC Ensembl
Innerchr13:35209520..35219778hg19UCSC Ensembl
Innerchr13:34107520..34117778hg18UCSC Ensembl
Innerchr13:34107520..34117778hg17UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg3810259
hg1910259
hg1810259
hg1710259
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700907
Samples
Known GenesLINC00457
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524898
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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