A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16984249



Internal ID56874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:77495264..77501085hg38UCSC Ensembl
chr6:78204981..78210802hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg385822
hg195822
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5463246
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16984249
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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