A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4745897



Internal ID20521908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45229198..45229327hg38UCSC Ensembl
chr19:45732456..45732585hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16287162
Samples
Known GenesEXOC3L2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4745897
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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