A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2761194



Internal ID17766796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4410360..4467799hg38UCSC Ensembl
Innerchr11:4431590..4489029hg19UCSC Ensembl
Innerchr11:4388166..4445605hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3857440
hg1957440
hg1857440
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv976509
Supporting Variants
SamplesHGDP00542
Known GenesOR52K2
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2761194
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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