A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4735601



Internal ID20511545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39468724..39469000hg38UCSC Ensembl
chr3:39510215..39510491hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16282225
Samples
Known GenesMOBP
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4735601
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