A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364739



Internal ID21022292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:152858128..152858765hg38UCSC Ensembl
chr3:152575917..152576554hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38638
hg19638
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096749
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364739
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