A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17608133



Internal ID21800180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:44411830..44411909hg38UCSC Ensembl
chr13:44985966..44986045hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6030620
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17608133
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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