A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533936



Internal ID20907297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16596401..16602400hg38UCSC Ensembl
chr19:16707212..16713211hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg386000
hg196000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044492
Samples
Known GenesMED26
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533936
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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