A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16982476



Internal ID55676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29574023..29588066hg38UCSC Ensembl
chr6:29541800..29555843hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3814044
hg1914044
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5463813
Supporting Variants
Samples
Known GenesOR2H2, SNORD32B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16982476
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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