A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765323



Internal ID20541183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:179737818..179737818hg38UCSC Ensembl
chr5:179164819..179164819hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288018
Samples
Known GenesMAML1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765323
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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