A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857189



Internal ID22632124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:3849771..3852996hg38UCSC Ensembl
chr12:3958937..3962162hg19UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg383226
hg193226
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv320n209
Supporting Variantsnssv17461629
Samples
Known GenesPARP11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857189
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