A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859355



Internal ID22634290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:121490312..121491587hg38UCSC Ensembl
chr12:121928115..121929390hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg381276
hg191276
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17460625
Samples
Known GenesKDM2B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859355
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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