A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1142995



Internal ID19268941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:62105822..62105930hg38UCSC Ensembl
Outerchr20:60680878..60680986hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2282n106
Supporting Variantsnssv3979766
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1142995
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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