A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528788



Internal ID15456081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:37322896..37356774hg38UCSC Ensembl
Innerchr11:37344446..37378324hg19UCSC Ensembl
Innerchr11:37301022..37334900hg18UCSC Ensembl
Innerchr11:37301022..37334900hg17UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3833879
hg1933879
hg1833879
hg1733879
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705458
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528788
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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