A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16981735



Internal ID55180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:45826116..45827344hg38UCSC Ensembl
chr6:45793853..45795081hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg381229
hg191229
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5470917
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16981735
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00281


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