A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14090152



Internal ID21269322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:32346002..32349468hg38UCSC Ensembl
Innerchr10:32634930..32638396hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg383467
hg193467
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114786
Supporting Variants
Samplessample138
Known GenesEPC1, LOC102031319
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14090152
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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