A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5515599



Internal ID292080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9423177..9434916hg38UCSC Ensembl
chr19:9533853..9545592hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3811740
hg1911740
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17721225
Samples
Known GenesZNF266
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5515599
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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