A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848999



Internal ID22623934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:107370569..107378840hg38UCSC Ensembl
chr10:109130327..109138598hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg388272
hg198272
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17454978
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848999
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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