A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5912253



Internal ID22687469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69471214..69478252hg38UCSC Ensembl
chr10:71230970..71238008hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg387039
hg197039
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17349826
Samples
Known GenesTSPAN15
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5912253
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