A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862642



Internal ID22637577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:119962749..119965901hg38UCSC Ensembl
chr12:120400553..120403705hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg383153
hg193153
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17452249
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862642
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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