A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4762934



Internal ID20538794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:24937873..24937873hg38UCSC Ensembl
chr13:25512011..25512011hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16276427
Samples
Known GenesTPTE2P1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4762934
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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