A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531190



Internal ID20904551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:53414823..53497556hg38UCSC Ensembl
chr19:53918076..54000810hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3882734
hg1982735
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3712n223
Supporting Variantsnssv18200181
Samples
Known GenesTPM3P9, ZNF761, ZNF813
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531190
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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