A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6408446



Internal ID21065999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:155766740..155767309hg38UCSC Ensembl
chr5:155193750..155194319hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg38570
hg19570
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18129435
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6408446
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