A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859085



Internal ID22634020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:62106227..62108822hg38UCSC Ensembl
chr12:62500008..62502603hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg382596
hg192596
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv418n209
Supporting Variantsnssv17463679
Samples
Known GenesFAM19A2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859085
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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