A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520577



Internal ID20893938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11350450..11379379hg38UCSC Ensembl
chr19:11461126..11490055hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3828930
hg1928930
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198062
Samples
Known GenesCCDC159, EPOR, LPPR2, SWSAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520577
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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