A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437149



Internal ID21094702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:65796421..65809906hg38UCSC Ensembl
chr10:67556179..67569664hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3813486
hg1913486
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189090
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437149
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