A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3959052



Internal ID19210591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:19799847..19815647hg38UCSC Ensembl
Outerchr15:20005100..20020900hg19UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3815801
hg1915801
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1118543
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3959052
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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