A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14090106



Internal ID21267818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:58512288..58514427hg38UCSC Ensembl
Innerchr10:60272048..60274187hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg382140
hg192140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111235
Supporting Variants
Samplessample117
Known GenesBICC1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14090106
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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