A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464873



Internal ID21122426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62726701..62728500hg38UCSC Ensembl
chr11:62494173..62495972hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186503
Samples
Known GenesHNRNPUL2, HNRNPUL2-BSCL2, TTC9C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464873
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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