A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5476763



Internal ID254368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43463845..43473147hg38UCSC Ensembl
chr10:43959293..43968595hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg389303
hg199303
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17032769
Samples
Known GenesZNF487
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5476763
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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