A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3983955



Internal ID18894789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:42349587..42349737hg38UCSC Ensembl
Outerchr21:43769696..43769846hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1125746
Supporting Variants
SamplesKWS2
Known GenesTFF2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3983955
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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