A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16978840



Internal ID53274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:4990546..4990790hg38UCSC Ensembl
chr6:4990780..4991024hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38245
hg19245
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5466404
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16978840
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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