A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861789



Internal ID22636724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121140899..121148898hg38UCSC Ensembl
chr10:122900413..122908412hg19UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg388000
hg198000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458723, nssv17465394
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861789
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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