A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16264053



Internal ID20473271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:88593407..88593564hg38UCSC Ensembl
chr11:88326575..88326732hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38158
hg19158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4749349
Supporting Variants
Samples
Known GenesGRM5
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16264053
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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