A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852022



Internal ID22626957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:121589473..121592827hg38UCSC Ensembl
chr12:122027378..122030732hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg383355
hg193355
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17462637
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852022
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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