A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5902817



Internal ID22677978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:28416921..28417052hg38UCSC Ensembl
chr6:28384698..28384829hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444729
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5902817
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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