A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16989289



Internal ID60282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:148305478..148308905hg38UCSC Ensembl
chr6:148626614..148630041hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg383428
hg193428
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5471140
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16989289
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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