A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5919023



Internal ID22694245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72512299..72531148hg38UCSC Ensembl
chr11:72223343..72242192hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3818850
hg1918850
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17363964
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5919023
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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