A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862193



Internal ID22637128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:45141160..45143359hg38UCSC Ensembl
chr12:45534943..45537142hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458374
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862193
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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