A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5916192



Internal ID22691411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:58783971..58876146hg38UCSC Ensembl
chr11:58551444..58643619hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3892176
hg1992176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17368492
Samples
Known GenesGLYATL2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5916192
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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