A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18044308



Internal ID20611348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10480401..10485700hg38UCSC Ensembl
chr19:10591077..10596376hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg385300
hg195300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6523129
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18044308
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00123


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