A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730828



Internal ID20506743
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 StatusM
Merged Variants
Supporting Variantsnssv16279923
Samples
Known GenesT
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4730828
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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