A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552028



Internal ID20925158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:35221521..35224235hg38UCSC Ensembl
chr21:36593818..36596532hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg382715
hg192715
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072137
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552028
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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