A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5924459



Internal ID22699686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:35955633..37397649hg38UCSC Ensembl
chr10:36244561..37686577hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg381442017
hg191442017
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17356949
Samples
Known GenesANKRD30A, LINC00993
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5924459
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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