A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18047325



Internal ID20614365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:21550320..21645404hg38UCSC Ensembl
chr19:21733122..21828206hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg3895085
hg1995085
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6528588
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18047325
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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