A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1133304



Internal ID18901328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:63731357..63731622hg38UCSC Ensembl
Outerchr20:62362709..62362974hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2293n106
Supporting Variantsnssv3988219
SamplesKWS1
Known GenesZGPAT
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1133304
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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