A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14097535



Internal ID21274491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34944910..34953116hg38UCSC Ensembl
Innerchr15:35237111..35245317hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg388207
hg198207
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117259
Supporting Variants
Samplessample208
Known GenesAQR
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14097535
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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