A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4758309



Internal ID20534169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110043587..110043587hg38UCSC Ensembl
chr13:110695934..110695934hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38186
hg19186
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16270851
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4758309
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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