A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526167



Internal ID20899528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6110525..6112786hg38UCSC Ensembl
chr19:6110536..6112797hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg382262
hg192262
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198977
Samples
Known GenesRFX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526167
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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