A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17041670



Internal ID95486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:4912950..4915854hg38UCSC Ensembl
chr11:4934180..4937084hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg382905
hg192905
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5496438
Supporting Variants
Samples
Known GenesOR51G2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17041670
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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