A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532642



Internal ID20906003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58091835..58168844hg38UCSC Ensembl
chr19:58603202..58680211hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3877010
hg1977010
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198341
Samples
Known GenesZNF329, ZSCAN18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532642
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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