A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362445



Internal ID21019998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:25061301..25062300hg38UCSC Ensembl
chr3:25102792..25103791hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101091
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362445
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