A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18045120



Internal ID20612160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:18786230..18791907hg38UCSC Ensembl
chr19:18897040..18902716hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg385678
hg195677
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6519673
Supporting Variants
Samples
Known GenesCOMP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18045120
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00048


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