A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18050094



Internal ID20617134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9004381..9023818hg38UCSC Ensembl
chr19:9115057..9134494hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3819438
hg1919438
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6516731
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18050094
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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