A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861129



Internal ID22636064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:112047722..112049221hg38UCSC Ensembl
chr12:112485526..112487025hg19UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17450704
Samples
Known GenesNAA25
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861129
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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