A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5916099



Internal ID22691318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63982007..63984993hg38UCSC Ensembl
chr11:63749479..63752465hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg382987
hg192987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv267n209
Supporting Variantsnssv17354426
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5916099
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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