A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4751891



Internal ID20527751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:70376526..70376526hg38UCSC Ensembl
chr15:70668865..70668865hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16279719
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4751891
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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