A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199658



Internal ID20766698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55904564..56334872hg38UCSC Ensembl
chr19:56415930..56846241hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38430309
hg19430312
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6522882
Supporting Variants
Samples
Known GenesGALP, NLRP13, NLRP5, NLRP8, ZNF444, ZNF787, ZSCAN5A, ZSCAN5B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199658
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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