A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369223



Internal ID21026776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:178173850..178174252hg38UCSC Ensembl
chr3:177891638..177892040hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg38403
hg19403
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18098798
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369223
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