A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113323



Internal ID21296589
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 StatusM
Merged Variantsdgv507n145
Supporting Variantsnssv14098959
Samplessample176
Known GenesCOG1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113323
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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