A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866253



Internal ID22641188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:81176120..81186676hg38UCSC Ensembl
chr10:82935876..82946432hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3810557
hg1910557
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17466341
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866253
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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