A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523832



Internal ID20897193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8670709..8673647hg38UCSC Ensembl
chr19:8780543..8783482hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg382939
hg192940
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18050069
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523832
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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