A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525805



Internal ID20899166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55705026..55812457hg38UCSC Ensembl
chr19:56216392..56323823hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38107432
hg19107432
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199640
Samples
Known GenesNLRP11, NLRP9, RFPL4A, RFPL4AL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525805
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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