A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850909



Internal ID22625844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:51048282..51051181hg38UCSC Ensembl
chr12:51442065..51444964hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg382900
hg192900
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv411n209
Supporting Variantsnssv17453738
Samples
Known GenesLETMD1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850909
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