A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765864



Internal ID20541724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:62893481..62893481hg38UCSC Ensembl
chr15:63185680..63185680hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16279247
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765864
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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