A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4754075



Internal ID20529935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155938943..155938943hg38UCSC Ensembl
chr3:155656732..155656732hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg381164
hg191164
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16282233
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4754075
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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