A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1129665



Internal ID19282512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:62105808..62105912hg38UCSC Ensembl
Outerchr20:60680864..60680968hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2282n106
Supporting Variantsnssv3963954
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1129665
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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