A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859884



Internal ID22634819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119180124..119184102hg38UCSC Ensembl
chr10:120939636..120943614hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg383979
hg193979
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17464646
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859884
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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