A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859066



Internal ID22634001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:50067312..50068511hg38UCSC Ensembl
chr12:50461095..50462294hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17467115, nssv17459201
Samples
Known GenesASIC1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859066
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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