A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920167



Internal ID22695390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64310328..64311785hg38UCSC Ensembl
chr11:64077800..64079257hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg381458
hg191458
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17351227
Samples
Known GenesESRRA
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920167
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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