A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14090250



Internal ID21286977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:19119940..19122539hg38UCSC Ensembl
Innerchr11:19141487..19144086hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112600
Supporting Variants
Samplessample396
Known GenesZDHHC13
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14090250
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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