A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451190



Internal ID21108743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43443225..43480512hg38UCSC Ensembl
chr10:43938673..43975960hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3837288
hg1937288
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17981650
Samples
Known GenesZNF487
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451190
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