A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16277653



Internal ID20486871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:87801976..87802153hg38UCSC Ensembl
chr3:87851126..87851303hg19UCSC Ensembl
Cytoband3p11.2
Allele length
AssemblyAllele length
hg38178
hg19178
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4747930
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16277653
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