A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16278015



Internal ID20487233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1554309..1554421hg38UCSC Ensembl
chr11:1575539..1575651hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4739385
Supporting Variants
Samples
Known GenesDUSP8, MOB2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16278015
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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