A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856693



Internal ID22631628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:111033424..111037368hg38UCSC Ensembl
chr12:111471228..111475172hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg383945
hg193945
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463629
Samples
Known GenesCUX2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856693
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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