A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14088729



Internal ID21279741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5663904..5667568hg38UCSC Ensembl
Innerchr10:5705867..5709531hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg383665
hg193665
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111548
Supporting Variants
Samplessample289
Known GenesASB13
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14088729
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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