A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364515



Internal ID21022068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:173206834..173207444hg38UCSC Ensembl
chr3:172924624..172925234hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38611
hg19611
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18098845
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364515
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