A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17388281



Internal ID22446151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:60931543..60933001hg38UCSC Ensembl
chr13:61505677..61507135hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg381459
hg191459
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5928438
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17388281
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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