A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16263040



Internal ID20472258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:58538195..58538530hg38UCSC Ensembl
chr11:58305668..58306003hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4735247
Supporting Variants
Samples
Known GenesLPXN
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16263040
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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