A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523994



Internal ID20897355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17517626..17533338hg38UCSC Ensembl
chr19:17628435..17644147hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3815713
hg1915713
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197703
Samples
Known GenesFAM129C, PGLS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523994
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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