A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4002988



Internal ID19190225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:37469798..37475799hg38UCSC Ensembl
Outerchr15:37761999..37768000hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg386002
hg196002
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1151565
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4002988
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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