A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18137962



Internal ID20705002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:119785388..119793528hg38UCSC Ensembl
chr6:120106534..120114674hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg388141
hg198141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6603474
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18137962
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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