A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861045



Internal ID22635980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:83585483..83590473hg38UCSC Ensembl
chr12:83979262..83984252hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg384991
hg194991
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17459569
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861045
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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