A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155710



Internal ID22086215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:17653017..17802664hg38UCSC Ensembl
Outerchr21:17645849..17811396hg38UCSC Ensembl
Innerchr21:19025335..19174981hg19UCSC Ensembl
Outerchr21:19018167..19183713hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38165548
hg19165547
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4014801
Samples
Known GenesC21orf91, C21orf91-OT1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155710
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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