A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855006



Internal ID22629941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:109185994..109188643hg38UCSC Ensembl
chr12:109623799..109626448hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg382650
hg192650
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17457443
Samples
Known GenesACACB
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855006
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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