A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18045303



Internal ID20612343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:23360532..23360999hg38UCSC Ensembl
chr19:23543334..23543801hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38468
hg19468
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6516534
Supporting Variants
Samples
Known GenesZNF91
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18045303
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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