A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925826



Internal ID22701053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1643452..1645465hg38UCSC Ensembl
chr11:1664682..1666695hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg382014
hg192014
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17368049
Samples
Known GenesMOB2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925826
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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