A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520273



Internal ID20893634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12386121..12425768hg38UCSC Ensembl
chr19:12496935..12536582hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3839648
hg1939648
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3443n223
Supporting Variantsnssv18197342
Samples
Known GenesZNF799
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520273
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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