A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865261



Internal ID22640196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:122152273..122163061hg38UCSC Ensembl
chr12:122636820..122647608hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg3810789
hg1910789
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv455n209
Supporting Variantsnssv17463609
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865261
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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