A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848316



Internal ID22623251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89347251..89363783hg38UCSC Ensembl
chr10:91107008..91123540hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3816533
hg1916533
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17466670
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848316
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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