A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516173



Internal ID20889534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:53399019..53402759hg38UCSC Ensembl
chr19:53902272..53906012hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg383741
hg193741
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046972
Samples
Known GenesZNF765
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516173
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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