A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5933787



Internal ID22709103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57211868..57212119hg38UCSC Ensembl
chr19:57723236..57723487hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38252
hg19252
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17399655
Samples
Known GenesZNF264
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5933787
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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