A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851867



Internal ID22626802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:55578465..55581032hg38UCSC Ensembl
chr12:55972249..55974816hg19UCSC Ensembl
Cytoband12q13.2
Allele length
AssemblyAllele length
hg382568
hg192568
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17450777
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851867
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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