A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189822



Internal ID20756862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7714633..7908708hg38UCSC Ensembl
chr11:7736180..7930255hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38194076
hg19194076
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6437319
Supporting Variants
Samples
Known GenesLOC283299, OR5E1P, OR5P2, OR5P3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189822
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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