A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3999895



Internal ID19188756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:101976196..101979697hg38UCSC Ensembl
Outerchr15:102516399..102519900hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg383502
hg193502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1152713
Supporting Variants
SamplesKWB1
Known GenesDDX11L9, WASH3P
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3999895
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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