A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530599



Internal ID20903960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:52319886..52344851hg38UCSC Ensembl
chr19:52823139..52848104hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3824966
hg1924966
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198329
Samples
Known GenesZNF480, ZNF610
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530599
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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