A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861036



Internal ID22635971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:132758815..132762682hg38UCSC Ensembl
chr12:133335401..133339268hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg383868
hg193868
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17467884
Samples
Known GenesANKLE2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861036
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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