A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766766



Internal ID20542626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24730301..24730301hg38UCSC Ensembl
chr1:25056792..25056792hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38214
hg19214
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16264569
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766766
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer