A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407394



Internal ID21064947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:64694397..64697118hg38UCSC Ensembl
chr5:63990224..63992945hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg382722
hg192722
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18132104
Samples
Known GenesFAM159B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407394
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