A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362273



Internal ID21019826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:24971905..25035138hg38UCSC Ensembl
chr3:25013396..25076629hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3863234
hg1963234
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101083
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362273
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