A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761085



Internal ID20536945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:63053805..63053805hg38UCSC Ensembl
chr1:63519476..63519476hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285073
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761085
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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