A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524581



Internal ID20897942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:62410473..62415965hg38UCSC Ensembl
chr18:60077706..60083198hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg385493
hg195493
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18043362
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524581
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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