A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4745254



Internal ID20521260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109717277..109717403hg38UCSC Ensembl
chr13:110369624..110369750hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275191
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4745254
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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