A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18044280



Internal ID20611320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10216374..10217652hg38UCSC Ensembl
chr19:10327050..10328328hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381279
hg191279
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6530815
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18044280
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00019


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