A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18047380



Internal ID20614420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:31028401..31029800hg38UCSC Ensembl
chr19:31519307..31520706hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6524241
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18047380
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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