A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4752651



Internal ID20528511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8026884..8026884hg38UCSC Ensembl
chr1:8086944..8086944hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16278461
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4752651
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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