A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16279923



Internal ID20489141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166162680..166162807hg38UCSC Ensembl
chr6:166576168..166576295hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730828
Supporting Variants
Samples
Known GenesT
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16279923
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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