A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14109337



Internal ID21270290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:51517095..51520953hg38UCSC Ensembl
Innerchr1:51982767..51986625hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg383859
hg193859
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117445
Supporting Variants
Samplessample149
Known GenesEPS15
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14109337
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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