A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444831



Internal ID21102384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11778469..11803231hg38UCSC Ensembl
chr10:11820468..11845230hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3824763
hg1924763
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196236
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444831
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