A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155104



Internal ID22085609
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 Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4009793, nssv4009792
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155104
Frequency
Sample Size131
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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