A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16979473



Internal ID53697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:9494456..9494765hg38UCSC Ensembl
chr6:9494689..9494998hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5465738
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16979473
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0128


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