A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16289781



Internal ID20498999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:147909568..147909568hg38UCSC Ensembl
chr6:148230704..148230704hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4765588
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16289781
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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