A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5921874



Internal ID22697098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:26306719..26307690hg38UCSC Ensembl
chr11:26328266..26329237hg19UCSC Ensembl
Cytoband11p14.2
Allele length
AssemblyAllele length
hg38972
hg19972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17353135
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5921874
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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