A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18044492



Internal ID20611532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16596401..16602400hg38UCSC Ensembl
chr19:16707212..16713211hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg386000
hg196000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6533936
Supporting Variants
Samples
Known GenesMED26
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18044492
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00025


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