A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18046388



Internal ID20613428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:42227323..42227662hg38UCSC Ensembl
chr19:42731475..42731814hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38340
hg19340
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6528757
Supporting Variants
Samples
Known GenesZNF526
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18046388
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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