A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908972



Internal ID22684182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86534155..86536997hg38UCSC Ensembl
chr10:88293912..88296754hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg382843
hg192843
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17350270
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908972
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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