A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089029



Internal ID21290562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:107646795..107651627hg38UCSC Ensembl
Innerchr10:109406553..109411385hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg384833
hg194833
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110923
Supporting Variants
Samplessample60
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089029
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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