A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117972



Internal ID21301238
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 StatusM
Merged Variants
Supporting Variantsnssv14094280
Samplessample111
Known GenesELMSAN1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117972
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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