A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6065398



Internal ID21974631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:151031300..151031300hg38UCSC Ensembl
chr3:150749087..150749087hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38453
hg19453
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17543525
Samples
Known GenesCLRN1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6065398
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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