A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14096231



Internal ID21272574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:26502719..26507187hg38UCSC Ensembl
Innerchr15:26747866..26752334hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg384469
hg194469
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116469
Supporting Variants
Samplessample179
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14096231
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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