A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521680



Internal ID20895041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17817328..17825772hg38UCSC Ensembl
chr19:17928137..17936581hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg388445
hg198445
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197709
Samples
Known GenesINSL3, JAK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521680
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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