A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525646



Internal ID20899007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16886123..16942236hg38UCSC Ensembl
chr19:16996934..17053046hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3856114
hg1956113
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197684
Samples
Known GenesCPAMD8, F2RL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525646
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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