A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191853



Internal ID20758893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47685222..48644097hg38UCSC Ensembl
chr11:47706774..48665649hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38958876
hg19958876
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6463105
Supporting Variants
Samples
Known GenesAGBL2, FNBP4, NUP160, OR4A47, OR4B1, OR4C3, OR4C45, OR4S1, OR4X1, OR4X2, PTPRJ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191853
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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