A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447092



Internal ID21104645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43451201..43470600hg38UCSC Ensembl
chr10:43946649..43966048hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3819400
hg1919400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17981652
Samples
Known GenesZNF487
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447092
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