A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18139069



Internal ID20706109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:146685696..146686068hg38UCSC Ensembl
chr6:147006832..147007204hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg38373
hg19373
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6608502
Supporting Variants
Samples
Known GenesADGB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18139069
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00117


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