A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4762410



Internal ID20538270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:46377725..46377725hg38UCSC Ensembl
chr4:46379742..46379742hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg38263
hg19263
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16259054
Samples
Known GenesGABRA2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4762410
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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