A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865198



Internal ID22640133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:3826320..3832041hg38UCSC Ensembl
chr12:3935486..3941207hg19UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg385722
hg195722
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17453302
Samples
Known GenesPARP11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865198
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