A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16980827



Internal ID54585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24957559..24970679hg38UCSC Ensembl
chr6:24957787..24970907hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3813121
hg1913121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5455502
Supporting Variants
Samples
Known GenesFAM65B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16980827
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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