A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18197417



Internal ID20764457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15209584..15212453hg38UCSC Ensembl
chr19:15320395..15323264hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg382870
hg192870
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6519894
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18197417
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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