A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14086813



Internal ID21284388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:27099330..27115322hg38UCSC Ensembl
Innerchr7:27138949..27154941hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3815993
hg1915993
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114685
Supporting Variants
Samplessample360
Known GenesHOTAIRM1, HOXA2, HOXA3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14086813
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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