A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16276362



Internal ID20485580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:192828601..192828661hg38UCSC Ensembl
chr3:192546390..192546450hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4744492
Supporting Variants
Samples
Known GenesMB21D2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16276362
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