A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861724



Internal ID22636659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:83402615..83405893hg38UCSC Ensembl
chr12:83796394..83799672hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg383279
hg193279
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17454377, nssv17460353
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861724
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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