A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866262



Internal ID22641197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:91182051..91183150hg38UCSC Ensembl
chr12:91575828..91576927hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17454264
Samples
Known GenesDCN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866262
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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