A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524651



Internal ID15105258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:121070874..121084060hg38UCSC Ensembl
Innerchr11:120941583..120954769hg19UCSC Ensembl
Innerchr11:120446793..120459979hg18UCSC Ensembl
Innerchr11:120446793..120459979hg17UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3813187
hg1913187
hg1813187
hg1713187
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700618
Samples
Known GenesTBCEL
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524651
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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