A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14088937



Internal ID21269475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:25873167..25877332hg38UCSC Ensembl
Innerchr10:26162096..26166261hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg384166
hg194166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111866
Supporting Variants
Samplessample14
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14088937
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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