A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765603



Internal ID20541463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:145891285..145891285hg38UCSC Ensembl
chr2:146648853..146648853hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16279573
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765603
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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