A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14098083



Internal ID21290900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:14836104..14898443hg38UCSC Ensembl
Innerchr17:14739421..14801760hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3862340
hg1962340
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115126
Supporting Variants
Samplessample66
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14098083
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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