A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111928



Internal ID21295194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:35596399..35598128hg38UCSC Ensembl
Innerchr17:33923418..33925147hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg381730
hg191730
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14098872
Samplessample136
Known GenesAP2B1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111928
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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