A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853990



Internal ID22628925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:77371758..77375880hg38UCSC Ensembl
chr12:77765538..77769660hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg384123
hg194123
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv427n209
Supporting Variantsnssv17463986, nssv17460894
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853990
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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