A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526034



Internal ID15453327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:19027931..19054080hg38UCSC Ensembl
Innerchr11:19049478..19075627hg19UCSC Ensembl
Innerchr11:19006054..19032203hg18UCSC Ensembl
Innerchr11:19006054..19032203hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3826150
hg1926150
hg1826150
hg1726150
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702265
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526034
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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