A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862824



Internal ID22637759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110464649..110472048hg38UCSC Ensembl
chr12:110902454..110909853hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg387400
hg197400
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17465628
Samples
Known GenesFAM216A, GPN3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862824
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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