A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16274974



Internal ID20484192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86025283..86025343hg38UCSC Ensembl
chr11:85736325..85736385hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4749803
Supporting Variants
Samples
Known GenesPICALM
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16274974
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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