A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859360



Internal ID22634295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:3849772..3853822hg38UCSC Ensembl
chr12:3958938..3962988hg19UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg384051
hg194051
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv320n209
Supporting Variantsnssv17449923
Samples
Known GenesPARP11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859360
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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