A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960021



Internal ID19207998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:31216079..31245697hg38UCSC Ensembl
Outerchr20:29803900..29833500hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3829619
hg1929601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1110370
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960021
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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