A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534616



Internal ID20907977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:18372180..18374912hg38UCSC Ensembl
chr19:18482990..18485722hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg382733
hg192733
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045097
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534616
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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