A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856092



Internal ID22631027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:133234283..133237018hg38UCSC Ensembl
chr12:133810869..133813604hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg382736
hg192736
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455648, nssv17450260
Samples
Known GenesANHX
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856092
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer