A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5915357



Internal ID22690575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:128784109..128787349hg38UCSC Ensembl
chr10:130582373..130585613hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg383241
hg193241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17352233
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5915357
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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