A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445060



Internal ID21102613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11692090..11702203hg38UCSC Ensembl
chr10:11734089..11744202hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3810114
hg1910114
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189427
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445060
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