A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852139



Internal ID22627074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110473249..110476015hg38UCSC Ensembl
chr12:110911054..110913820hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg382767
hg192767
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17461326, nssv17450405
Samples
Known GenesFAM216A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852139
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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