A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760782



Internal ID20536642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:96541060..96541060hg38UCSC Ensembl
chr15:97084290..97084290hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16296039
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760782
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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