A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526943



Internal ID15107550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:109741130..109769537hg38UCSC Ensembl
Innerchr13:110393477..110421884hg19UCSC Ensembl
Innerchr13:109191478..109219885hg18UCSC Ensembl
Innerchr13:109191478..109219885hg17UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3828408
hg1928408
hg1828408
hg1728408
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703313
Samples
Known GenesIRS2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526943
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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