A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5513578



Internal ID290097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3598372..3731278hg38UCSC Ensembl
chr11:3619602..3752508hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38132907
hg19132907
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17043122
Samples
Known GenesART1, ART5, CHRNA10, NUP98, TRPC2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5513578
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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