A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765882



Internal ID20541742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:172308907..172308907hg38UCSC Ensembl
chr5:171735911..171735911hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16291588
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765882
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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