A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16980709



Internal ID54520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:19175436..19180472hg38UCSC Ensembl
chr6:19175667..19180703hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg385037
hg195037
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5460362
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16980709
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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