A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1150562



Internal ID19198833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:113446384..113447685hg38UCSC Ensembl
Outerchr13:114100699..114102000hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381302
hg191302
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3996037
SamplesKWB1
Known GenesADPRHL1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1150562
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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