A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860194



Internal ID22635129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:130024780..130028894hg38UCSC Ensembl
chr11:129894675..129898789hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg384115
hg194115
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv295n209
Supporting Variantsnssv17469494, nssv17468040
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860194
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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