A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117652



Internal ID21300918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:19866986..19868956hg38UCSC Ensembl
Innerchr17:19770299..19772269hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg381971
hg191971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv484n145
Supporting Variantsnssv14097673, nssv14098125
Samplessample224, sample86
Known GenesULK2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117652
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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