A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6473700



Internal ID21131253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:129868637..129869579hg38UCSC Ensembl
chr11:129738532..129739474hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38943
hg19943
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192634
Samples
Known GenesNFRKB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6473700
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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