A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4753232



Internal ID20529092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:52064222..52064222hg38UCSC Ensembl
chr8:52976782..52976782hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16264395
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4753232
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