A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534182



Internal ID20907543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55699013..55700107hg38UCSC Ensembl
chr19:56210379..56211473hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg381095
hg191095
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18049210
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534182
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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