A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533702



Internal ID20907063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9766701..9769800hg38UCSC Ensembl
chr19:9877377..9880476hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg383100
hg193100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18049538
Samples
Known GenesZNF846
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533702
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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