A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463105



Internal ID21120658
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 StatusM
Merged Variants
Supporting Variantsnssv18191853
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)nsv6463105
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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