A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908089



Internal ID22683299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:45725805..45725863hg38UCSC Ensembl
chr11:45747356..45747414hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17356090
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908089
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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