A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1148857



Internal ID18854290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:61271727..61273128hg38UCSC Ensembl
Outerchr11:61039199..61040600hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg381402
hg191402
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3997644
SamplesKWB1
Known GenesVWCE
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1148857
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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