A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16280334



Internal ID20489552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11117334..11117334hg38UCSC Ensembl
chr6:11117567..11117567hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4767731
Supporting Variants
Samples
Known GenesSMIM13
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16280334
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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