A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397698



Internal ID21055251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:72854126..72855649hg38UCSC Ensembl
chr5:72149953..72151476hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg381524
hg191524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18132173
Samples
Known GenesTNPO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397698
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