A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14088993



Internal ID21289274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:35430718..35433954hg38UCSC Ensembl
Innerchr10:35719646..35722882hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg383237
hg193237
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114328
Supporting Variants
Samplessample45
Known GenesCCNY
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14088993
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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