A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14094280



Internal ID21267359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73785947..73796177hg38UCSC Ensembl
Innerchr14:74252650..74262880hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3810231
hg1910231
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117972
Supporting Variants
Samplessample111
Known GenesELMSAN1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14094280
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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