A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14098550



Internal ID21283640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:57081476..57086509hg38UCSC Ensembl
Innerchr17:55158837..55163870hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg385034
hg195034
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110519
Supporting Variants
Samplessample348
Known GenesAKAP1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14098550
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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