A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17041812



Internal ID95576
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 StatusS
Merged Variantsnsv5510983
Supporting Variants
Samples
Known GenesLOC283299, OR5E1P, OR5P2, OR5P3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17041812
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000313


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