A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516534



Internal ID20889895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:23360532..23360999hg38UCSC Ensembl
chr19:23543334..23543801hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38468
hg19468
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045303
Samples
Known GenesZNF91
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516534
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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