A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199639



Internal ID20766679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55698809..55948499hg38UCSC Ensembl
chr19:56210175..56459865hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38249691
hg19249691
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6529699
Supporting Variants
Samples
Known GenesNLRP11, NLRP13, NLRP4, NLRP8, NLRP9, RFPL4A, RFPL4AL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199639
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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