A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530054



Internal ID20903415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38660472..38672584hg38UCSC Ensembl
chr19:39151112..39163224hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3812113
hg1912113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047813
Samples
Known GenesACTN4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530054
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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