A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4754869



Internal ID20530729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24219083..24219083hg38UCSC Ensembl
chr1:24545573..24545573hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16292645
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4754869
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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