A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3959686



Internal ID19206862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:62098741..62102941hg38UCSC Ensembl
Outerchr8:63011300..63015500hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg384201
hg194201
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1119250
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3959686
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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