A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920468



Internal ID22695691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60683572..60684257hg38UCSC Ensembl
chr11:60451045..60451730hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38686
hg19686
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17362574
Samples
Known GenesLINC00301
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920468
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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