A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14086763



Internal ID21283590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:27138117..27144462hg38UCSC Ensembl
Innerchr7:27177736..27184081hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg386346
hg196346
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114955
Supporting Variants
Samplessample346
Known GenesHOXA5, HOXA-AS3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14086763
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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