A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18138239



Internal ID20705279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:127512335..127512737hg38UCSC Ensembl
chr6:127833480..127833882hg19UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg38403
hg19403
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6611502
Supporting Variants
Samples
Known GenesSOGA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18138239
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00095


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