A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533413



Internal ID20906774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19835696..20400027hg38UCSC Ensembl
chr19:19946505..20510836hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38564332
hg19564332
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198386
Samples
Known GenesMIR1270-1, MIR1270-2, ZNF253, ZNF486, ZNF682, ZNF90, ZNF93
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533413
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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