A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5847813



Internal ID22622748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:130915075..130924907hg38UCSC Ensembl
chr12:131399620..131409452hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg389833
hg199833
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17457576
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5847813
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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