A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6466238



Internal ID21123791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:58783976..58876147hg38UCSC Ensembl
chr11:58551449..58643620hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3892172
hg1992172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17991966
Samples
Known GenesGLYATL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6466238
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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