A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730737



Internal ID20506651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:128328861..128329021hg38UCSC Ensembl
chr8:129341107..129341267hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16296583
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4730737
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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