A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908591



Internal ID22683801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87561868..87584416hg38UCSC Ensembl
chr10:89321625..89344173hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3822549
hg1922549
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17356233
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908591
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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