A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18050126



Internal ID20617166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9254964..9262659hg38UCSC Ensembl
chr19:9365640..9373335hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg387696
hg197696
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6519106
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18050126
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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