A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17043237



Internal ID96535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6149000..6190000hg38UCSC Ensembl
chr11:6170230..6211230hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3841001
hg1941001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5504520
Supporting Variants
Samples
Known GenesOR52B2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17043237
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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