A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517111



Internal ID20890472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6634158..6651176hg38UCSC Ensembl
chr19:6634169..6651187hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3817019
hg1917019
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18049671
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517111
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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