A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861792



Internal ID22636727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:25826085..25851822hg38UCSC Ensembl
chr10:26115014..26140751hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3825738
hg1925738
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17465320
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861792
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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