A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520265



Internal ID20893626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55906133..56077835hg38UCSC Ensembl
chr19:56417499..56589201hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38171703
hg19171703
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3774n223
Supporting Variantsnssv18199659
Samples
Known GenesNLRP13, NLRP5, NLRP8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520265
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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