A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4751144



Internal ID20527004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:108775531..108775531hg38UCSC Ensembl
chr10:110535289..110535289hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16283579
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4751144
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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