A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2766521



Internal ID17482704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:6478192..6497815hg38UCSC Ensembl
Innerchr11:6499422..6519045hg19UCSC Ensembl
Innerchr11:6455998..6475621hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3819624
hg1919624
hg1819624
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv972944
Supporting Variants
SamplesHGDP00998
Known GenesARFIP2, DNHD1, TIMM10B
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2766521
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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