A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3983938



Internal ID18899812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:63731348..63731615hg38UCSC Ensembl
Outerchr20:62362700..62362967hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1125731
Supporting Variants
SamplesKWS2
Known GenesZGPAT
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3983938
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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