A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3766225



Internal ID19312532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:22553596..22558897hg38UCSC Ensembl
chr15:23314199..23319500hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg385302
hg195302
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1078376
Supporting Variants
SamplesKWP1
Known GenesHERC2P2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3766225
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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