A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972951



Internal ID18261481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:67213004..67219265hg38UCSC Ensembl
Innerchr11:66980475..66986736hg19UCSC Ensembl
Innerchr11:66737051..66743312hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg386262
hg196262
hg186262
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2763115
SamplesHGDP00998
Known GenesKDM2A
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972951
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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