A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16979424



Internal ID53660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:5965521..5966633hg38UCSC Ensembl
chr6:5965754..5966866hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg381113
hg191113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5461641
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16979424
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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