A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14096002



Internal ID21290084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:27605141..27610592hg38UCSC Ensembl
Innerchr15:27850287..27855738hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg385452
hg195452
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110633
Supporting Variants
Samplessample55
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14096002
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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