A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531400



Internal ID20904761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:47124902..47145281hg38UCSC Ensembl
chr19:47628159..47648538hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3820380
hg1920380
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198935
Samples
Known GenesSAE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531400
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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