A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3118213



Internal ID21301479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:29632470..29634280hg38UCSC Ensembl
Innerchr17:27959488..27961298hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg381811
hg191811
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14098047
Samplessample55
Known GenesSSH2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3118213
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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