A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517794



Internal ID20891155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17691387..17707462hg38UCSC Ensembl
chr19:17802196..17818271hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3816076
hg1916076
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045032
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517794
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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