A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525636



Internal ID15106243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:112172891..112192531hg38UCSC Ensembl
Innerchr11:112043614..112063254hg19UCSC Ensembl
Innerchr11:111548824..111568464hg18UCSC Ensembl
Innerchr11:111548824..111568464hg17UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3819641
hg1919641
hg1819641
hg1719641
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701790
Samples
Known GenesBCO2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525636
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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