A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518920



Internal ID15099527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:76861972..76926607hg38UCSC Ensembl
Innerchr11:76573016..76637651hg19UCSC Ensembl
Innerchr11:76250664..76315299hg18UCSC Ensembl
Innerchr11:76250664..76315299hg17UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3864636
hg1964636
hg1864636
hg1764636
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696381
Samples
Known GenesACER3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518920
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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