A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4009792



Internal ID22071423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24201200..24233616hg38UCSC Ensembl
Outerchr15:24197072..24237898hg38UCSC Ensembl
Innerchr15:24446347..24478763hg19UCSC Ensembl
Outerchr15:24442219..24483045hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3840827
hg1940827
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155104
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4009792
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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