A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5487991



Internal ID265313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:35874603..35875833hg38UCSC Ensembl
chr10:36163531..36164761hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg381231
hg191231
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17033107
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5487991
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