A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112926



Internal ID21296192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:75225576..75246351hg38UCSC Ensembl
Innerchr17:73221671..73242432hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3820776
hg1920762
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14098868
Samplessample133
Known GenesGGA3, NUP85
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112926
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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