A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765138



Internal ID20540998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:169555621..169555621hg38UCSC Ensembl
chr1:169524859..169524859hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38618
hg19618
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16294474
Samples
Known GenesF5
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765138
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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