A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356764



Internal ID21014317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:101544478..101547596hg38UCSC Ensembl
chr3:101263322..101266440hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg383119
hg193119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18092401
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356764
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