A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859049



Internal ID22633984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:3985735..3991996hg38UCSC Ensembl
chr12:4094901..4101162hg19UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg386262
hg196262
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv322n209
Supporting Variantsnssv17451522
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859049
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