A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14088616



Internal ID21275712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:64753919..64834550hg38UCSC Ensembl
Innerchr10:66513676..66594307hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3880632
hg1980632
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115710
Supporting Variants
Samplessample226
Known GenesANXA2P3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14088616
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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