A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18140046



Internal ID20707086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:22200682..22258777hg38UCSC Ensembl
chr6:22200911..22259006hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3858096
hg1958096
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6412899
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18140046
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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