A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6054727



Internal ID21963961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:23950381..23950381hg38UCSC Ensembl
chr3:23991872..23991872hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg382582
hg192582
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17539744
Samples
Known GenesNR1D2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6054727
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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