A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3768972



Internal ID19304725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:101974396..101979397hg38UCSC Ensembl
chr15:102514599..102519600hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg385002
hg195002
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1076417
Supporting Variants
SamplesKWP1
Known GenesDDX11L9, WASH3P
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3768972
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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