A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5911997



Internal ID22687212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:24636823..24642802hg38UCSC Ensembl
chr11:24658369..24664348hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg385980
hg195980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17350356
Samples
Known GenesLUZP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5911997
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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