A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531466



Internal ID20904827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16447577..16448573hg38UCSC Ensembl
chr19:16558388..16559384hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38997
hg19997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044486
Samples
Known GenesEPS15L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531466
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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