A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857129



Internal ID22632064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:133238420..133243525hg38UCSC Ensembl
chr12:133815006..133820111hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg385106
hg195106
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv482n209
Supporting Variantsnssv17463517
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857129
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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