A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415225



Internal ID21072778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:131818268..131822842hg38UCSC Ensembl
chr5:131153961..131158535hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg384575
hg194575
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18125136
Samples
Known GenesLOC728637
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415225
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