A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4000210



Internal ID18845466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:46745601..46747102hg38UCSC Ensembl
Outerchr15:47037799..47039300hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg381502
hg191502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1147434
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4000210
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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