A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926239



Internal ID22701466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:122149355..122149541hg38UCSC Ensembl
chr11:122020063..122020249hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg38187
hg19187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17357210
Samples
Known GenesMIR100HG
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926239
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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