A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4763884



Internal ID20539744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:59769203..59769203hg38UCSC Ensembl
chr15:60061402..60061402hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16270428
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4763884
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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