A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3979769



Internal ID18892412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:63732347..63732424hg38UCSC Ensembl
Outerchr20:62363699..62363776hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1142997
Supporting Variants
SamplesKWS2
Known GenesZGPAT
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3979769
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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