A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16267445



Internal ID20476663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:60581607..60581704hg38UCSC Ensembl
chr13:61155741..61155838hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4749800
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16267445
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