A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18046074



Internal ID20613114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2790891..2793336hg38UCSC Ensembl
chr19:2790889..2793334hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg382446
hg192446
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6521270
Supporting Variants
Samples
Known GenesTHOP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18046074
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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