A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354141



Internal ID21011694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:3792424..3831631hg38UCSC Ensembl
chr2:3840014..3879221hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3839208
hg1939208
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089116
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354141
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