A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865080



Internal ID22640015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:91134640..91146347hg38UCSC Ensembl
chr12:91528417..91540124hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg3811708
hg1911708
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17456034
Samples
Known GenesDCN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865080
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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