A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860588



Internal ID22635523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60205202..60221194hg38UCSC Ensembl
chr11:59972675..59988667hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3815993
hg1915993
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17467364, nssv17453850
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860588
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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