A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851711



Internal ID22626646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:91177782..91180018hg38UCSC Ensembl
chr12:91571559..91573795hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg382237
hg192237
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17469564, nssv17452159
Samples
Known GenesDCN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851711
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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