A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521604



Internal ID20894965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10375901..10394700hg38UCSC Ensembl
chr19:10486577..10505376hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3818800
hg1918800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3437n223
Supporting Variantsnssv18198023
Samples
Known GenesCDC37, TYK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521604
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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