A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3962004



Internal ID19211323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:63847010..63847316hg38UCSC Ensembl
Outerchr20:62478363..62478669hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1120399
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3962004
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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