A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522225



Internal ID20895586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19876199..20790406hg38UCSC Ensembl
chr19:19987008..20973212hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38914208
hg19986205
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198387
Samples
Known GenesMIR1270-1, MIR1270-2, ZNF253, ZNF486, ZNF626, ZNF682, ZNF737, ZNF826P, ZNF90, ZNF93
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522225
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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