A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14083773



Internal ID21292019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:159725119..159729776hg38UCSC Ensembl
Innerchr6:160146151..160150808hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg384658
hg194658
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111340
Supporting Variants
Samplessample81
Known GenesWTAP
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14083773
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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