A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18044274



Internal ID20611314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10101601..10104000hg38UCSC Ensembl
chr19:10212277..10214676hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6534306
Supporting Variants
Samples
Known GenesANGPTL6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18044274
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.01499


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