A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv466n209



Internal ID22826541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:130875206..130876448hg38UCSC Ensembl
chr12:131359751..131360993hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg381243
hg191243
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5866997, nsv5847857
Samples
Known GenesRAN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv466n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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