A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14098868



Internal ID21269029
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 StatusS
Merged Variantsnsv3112926
Supporting Variants
Samplessample133
Known GenesGGA3, NUP85
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14098868
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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