A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18046578



Internal ID20613618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36530533..36567561hg38UCSC Ensembl
chr19:37021435..37058463hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3837029
hg1937029
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6528755
Supporting Variants
Samples
Known GenesZNF529
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18046578
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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