A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465546



Internal ID21123099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102285018..102287083hg38UCSC Ensembl
chr11:102155749..102157814hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg382066
hg192066
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985466
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465546
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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