A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16982457



Internal ID55663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29322946..29393541hg38UCSC Ensembl
chr6:29290723..29361318hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3870596
hg1970596
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5460731
Supporting Variants
Samples
Known GenesOR12D3, OR5V1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16982457
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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