A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6483071



Internal ID21140624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:72895953..72925098hg38UCSC Ensembl
chr13:73470091..73499236hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg3829146
hg1929146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18012812
Samples
Known GenesPIBF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6483071
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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