A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456019



Internal ID21113572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:122061075..122067443hg38UCSC Ensembl
chr11:121931783..121938151hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg386369
hg196369
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987615
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456019
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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