A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5912666



Internal ID22687882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15052262..15052880hg38UCSC Ensembl
chr10:15094261..15094879hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38619
hg19619
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17352901
Samples
Known GenesOLAH
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5912666
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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