A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3979763



Internal ID18897757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:43696486..43696990hg38UCSC Ensembl
Outerchr20:42325126..42325630hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38505
hg19505
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1117285
Supporting Variants
SamplesKWS2
Known GenesMYBL2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3979763
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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