A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438670



Internal ID21096223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28361678..28362405hg38UCSC Ensembl
chr10:28650607..28651334hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38728
hg19728
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190512
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438670
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer