A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454636



Internal ID21112189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:15798864..15799323hg38UCSC Ensembl
chr11:15820410..15820869hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38460
hg19460
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17989415
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454636
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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