A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14088581



Internal ID21274550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:43135843..43139732hg38UCSC Ensembl
Innerchr10:43631291..43635180hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg383890
hg193890
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115074
Supporting Variants
Samplessample208
Known GenesCSGALNACT2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14088581
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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