A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521986



Internal ID15449279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:94631195..94636039hg38UCSC Ensembl
Innerchr11:94364361..94369205hg19UCSC Ensembl
Innerchr11:94004009..94008853hg18UCSC Ensembl
Innerchr11:94004009..94008853hg17UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg384845
hg194845
hg184845
hg174845
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694753
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521986
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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