A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17041794



Internal ID95566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7515650..7976370hg38UCSC Ensembl
chr11:7536881..7997917hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38460721
hg19461037
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5500971
Supporting Variants
Samples
Known GenesCYB5R2, LOC283299, NLRP10, OR10A3, OR10A6, OR5E1P, OR5P2, OR5P3, OVCH2, PPFIBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17041794
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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