A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16263381



Internal ID20472599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73896947..73897039hg38UCSC Ensembl
chr11:73607992..73608084hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4731288
Supporting Variants
Samples
Known GenesPAAF1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16263381
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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