A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437745



Internal ID21095298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:33063666..33064070hg38UCSC Ensembl
chr10:33352594..33352998hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg38405
hg19405
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980118
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437745
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer