A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439616



Internal ID21097169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124885275..124889914hg38UCSC Ensembl
chr10:126573844..126578483hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg384640
hg194640
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178438
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439616
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