A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520477



Internal ID20893838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16793788..16796663hg38UCSC Ensembl
chr19:16904599..16907474hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg382876
hg192876
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044512
Samples
Known GenesNWD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520477
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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