A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16979299



Internal ID53572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:22911997..22918298hg38UCSC Ensembl
chr6:22912226..22918527hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg386302
hg196302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5462672
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16979299
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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