A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18007544



Internal ID20574584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:28271160..28271564hg38UCSC Ensembl
chr13:28845297..28845701hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg38405
hg19405
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6481807
Supporting Variants
Samples
Known GenesPAN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18007544
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00093


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