A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518740



Internal ID20892101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10954930..10960154hg38UCSC Ensembl
chr19:11065606..11070830hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg385225
hg195225
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044956
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518740
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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