A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5918366



Internal ID22693587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:58330267..58334882hg38UCSC Ensembl
chr10:60090027..60094642hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg384616
hg194616
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17366265
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5918366
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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