A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5916138



Internal ID22691357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68316140..68320744hg38UCSC Ensembl
chr11:68083608..68088212hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg384605
hg194605
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17360735
Samples
Known GenesLRP5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5916138
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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