A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532553



Internal ID20905914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58032831..58052639hg38UCSC Ensembl
chr19:58544199..58564007hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3819809
hg1919809
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198340
Samples
Known GenesZSCAN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532553
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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