A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4763253



Internal ID20539113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79905282..79905282hg38UCSC Ensembl
chr15:80197624..80197624hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38255
hg19255
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16279983
Samples
Known GenesST20, ST20-MTHFS
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4763253
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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