A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18140274



Internal ID20707314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:144346561..144348675hg38UCSC Ensembl
chr6:144667697..144669811hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg382115
hg192115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6608635
Supporting Variants
Samples
Known GenesUTRN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18140274
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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