A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14097037



Internal ID21277486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:67968613..67974770hg38UCSC Ensembl
Innerchr15:68260951..68267108hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg386158
hg196158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114181
Supporting Variants
Samplessample253
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14097037
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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