A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519914



Internal ID15100521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:86299747..86302319hg38UCSC Ensembl
Innerchr11:86010789..86013361hg19UCSC Ensembl
Innerchr11:85688437..85691009hg18UCSC Ensembl
Innerchr11:85688437..85691009hg17UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg382573
hg192573
hg182573
hg172573
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697122
Samples
Known GenesC11orf73
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519914
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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