A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5526068



Internal ID302212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19666594..19674436hg38UCSC Ensembl
chr19:19777403..19785245hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg387843
hg197843
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17722117
Samples
Known GenesZNF101
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5526068
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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