A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908645



Internal ID22683855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:58846467..59011722hg38UCSC Ensembl
chr11:58613940..58779195hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38165256
hg19165256
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv260n209
Supporting Variantsnssv17367679
Samples
Known GenesGLYATL1, LOC283194
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908645
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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