A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362792



Internal ID21020345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:38263993..38306547hg38UCSC Ensembl
chr3:38305484..38348038hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3842555
hg1942555
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100821
Samples
Known GenesSLC22A13, SLC22A14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362792
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