A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415190



Internal ID21072743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:150967679..150970847hg38UCSC Ensembl
chr5:150347241..150350409hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg383169
hg193169
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18128682
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415190
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