A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444294



Internal ID21101847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:118143417..118149104hg38UCSC Ensembl
chr10:119902928..119908615hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg385688
hg195688
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978349
Samples
Known GenesCASC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444294
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