A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5511084



Internal ID287683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112589071..112619799hg38UCSC Ensembl
chr10:114348830..114379558hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3830729
hg1930729
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17038163
Samples
Known GenesVTI1A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5511084
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