A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14090126



Internal ID21268273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:114265297..114273595hg38UCSC Ensembl
Innerchr10:116025056..116033354hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg388299
hg198299
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111533
Supporting Variants
Samplessample122
Known GenesVWA2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14090126
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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