A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854485



Internal ID22629420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110358443..110367864hg38UCSC Ensembl
chr12:110796248..110805669hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg389422
hg199422
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17456299
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854485
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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