A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18048146



Internal ID20615186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44177084..44177420hg38UCSC Ensembl
chr19:44681237..44681573hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6528066
Supporting Variants
Samples
Known GenesZNF226
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18048146
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00089


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