A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367207



Internal ID21024760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:31998387..32012996hg38UCSC Ensembl
chr3:32039879..32054488hg19UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg3814610
hg1914610
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099369
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367207
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