A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854971



Internal ID22629906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:80042143..80044789hg38UCSC Ensembl
chr12:80435923..80438569hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg382647
hg192647
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17460698
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854971
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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