A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441743



Internal ID21099296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:62725798..62735376hg38UCSC Ensembl
chr10:64485558..64495136hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg389579
hg199579
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193103
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441743
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