A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18138372



Internal ID20705412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:137977167..137985982hg38UCSC Ensembl
chr6:138298304..138307119hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg388816
hg198816
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6616648
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18138372
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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