A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5510983



Internal ID287588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7737600..7864000hg38UCSC Ensembl
chr11:7759147..7885547hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38126401
hg19126401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17041812
Samples
Known GenesLOC283299, OR5E1P, OR5P2, OR5P3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5510983
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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