A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469593



Internal ID21127146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59344998..59351629hg38UCSC Ensembl
chr11:59112471..59119102hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg386632
hg196632
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992437
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469593
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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