A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14085044



Internal ID21271823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:149852760..150125668hg38UCSC Ensembl
Innerchr7:149549849..149822757hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38272909
hg19272909
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113709
Supporting Variants
Samplessample169
Known GenesATP6V0E2, ATP6V0E2-AS1, ZNF862
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14085044
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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