A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3963968



Internal ID19221809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:17400211..17432581hg38UCSC Ensembl
Outerchr21:18772530..18804899hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3832371
hg1932370
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129674
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3963968
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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