A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534612



Internal ID20907973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58346644..58350121hg38UCSC Ensembl
chr19:58858010..58861487hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg383478
hg193478
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18049898
Samples
Known GenesA1BG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534612
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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