A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18046978



Internal ID20614018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:53422809..53503378hg38UCSC Ensembl
chr19:53926062..54006632hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3880570
hg1980571
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6527082
Supporting Variants
Samples
Known GenesTPM3P9, ZNF761, ZNF813
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18046978
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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