A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4763865



Internal ID20539725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:151031304..151031304hg38UCSC Ensembl
chr3:150749091..150749091hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16264962
Samples
Known GenesCLRN1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4763865
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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