A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526358



Internal ID20899719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:20119907..20234243hg38UCSC Ensembl
chr19:20230716..20345052hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38114337
hg19114337
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198401
Samples
Known GenesZNF486, ZNF90
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526358
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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