A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522205



Internal ID20895566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:47322023..47323077hg38UCSC Ensembl
chr19:47825280..47826334hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg381055
hg191055
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046888
Samples
Known GenesC5AR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522205
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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