A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18012811



Internal ID20579851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:72886601..72888400hg38UCSC Ensembl
chr13:73460739..73462538hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6490178
Supporting Variants
Samples
Known GenesPIBF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18012811
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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