A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866312



Internal ID22641247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:20102922..20105671hg38UCSC Ensembl
chr12:20255856..20258605hg19UCSC Ensembl
Cytoband12p12.2
Allele length
AssemblyAllele length
hg382750
hg192750
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17453931, nssv17460600
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866312
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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