A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16987796



Internal ID59304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:104456595..104490895hg38UCSC Ensembl
chr6:104904470..104938770hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3834301
hg1934301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5467995
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16987796
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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