A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4009749



Internal ID22071380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:19811075..19981398hg38UCSC Ensembl
Outerchr15:19811075..19985588hg38UCSC Ensembl
Innerchr15:20016328..20186651hg19UCSC Ensembl
Outerchr15:20016328..20190841hg19UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38174514
hg19174514
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155069
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4009749
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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