A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761091



Internal ID20536951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:176839753..176839753hg38UCSC Ensembl
chr2:177704481..177704481hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38775
hg19775
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265287
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761091
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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