A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851183



Internal ID22626118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45791277..45792510hg38UCSC Ensembl
chr10:46286725..46287958hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg381234
hg191234
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17466575, nssv17459831
Samples
Known GenesFAM21C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851183
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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