A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467683



Internal ID21125236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63541024..63546541hg38UCSC Ensembl
chr11:63308496..63314013hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg385518
hg195518
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993797
Samples
Known GenesMIR3680-1, MIR3680-2, RARRES3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467683
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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