A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18143177



Internal ID20710217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:20059848..20064175hg38UCSC Ensembl
chr6:20060079..20064406hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg384328
hg194328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6407317
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18143177
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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