A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865702



Internal ID22640637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:89503880..89504957hg38UCSC Ensembl
chr12:89897657..89898734hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg381078
hg191078
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458786
Samples
Known GenesPOC1B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865702
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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