A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369429



Internal ID21026982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:86893683..86894127hg38UCSC Ensembl
chr3:86942833..86943277hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg38445
hg19445
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18104133
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369429
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