A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522578



Internal ID20895939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16538576..16539365hg38UCSC Ensembl
chr19:16649387..16650176hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38790
hg19790
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044489
Samples
Known GenesCHERP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522578
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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