A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864259



Internal ID22639194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66680927..66688758hg38UCSC Ensembl
chr11:66448398..66456229hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg387832
hg197832
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17451796
Samples
Known GenesSPTBN2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864259
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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