A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5916515



Internal ID22691734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72772206..72772396hg38UCSC Ensembl
chr11:72483251..72483441hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38191
hg19191
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17354392
Samples
Known GenesSTARD10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5916515
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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