A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867158



Internal ID22642093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:68636087..68638746hg38UCSC Ensembl
chr12:69029867..69032526hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg382660
hg192660
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17468688, nssv17468480
Samples
Known GenesRAP1B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867158
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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