A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851095



Internal ID22626030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:113007155..113009354hg38UCSC Ensembl
chr12:113444960..113447159hg19UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455659
Samples
Known GenesOAS2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851095
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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