A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14095295



Internal ID21269460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:65304876..65323087hg38UCSC Ensembl
Innerchr15:65597214..65615425hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3818212
hg1918212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116666
Supporting Variants
Samplessample14
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14095295
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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