A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18046536



Internal ID20613576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45870021..45870408hg38UCSC Ensembl
chr19:46373279..46373666hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38388
hg19388
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6527271
Supporting Variants
Samples
Known GenesFOXA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18046536
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00012


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