A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761910



Internal ID20537770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:145617388..145617388hg38UCSC Ensembl
chr2:146374956..146374956hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16271776
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761910
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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