A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14098959



Internal ID21272332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:73190585..73196561hg38UCSC Ensembl
Innerchr17:71186724..71192700hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg385977
hg195977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113323
Supporting Variants
Samplessample176
Known GenesCOG1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14098959
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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