A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529057



Internal ID20902418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11874162..11958226hg38UCSC Ensembl
chr19:11984977..12069041hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3884065
hg1984065
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197335
Samples
Known GenesZNF69, ZNF700
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529057
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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