A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17611683



Internal ID21803730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:35694822..35697445hg38UCSC Ensembl
chr13:36268959..36271582hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg382624
hg192624
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6036364
Supporting Variants
Samples
Known GenesMIR548F5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17611683
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