A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5911794



Internal ID22687009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:128089023..128089860hg38UCSC Ensembl
chr10:129887287..129888124hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg38838
hg19838
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17355068
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5911794
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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