A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014098



Internal ID21923441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:165805052..165805126hg38UCSC Ensembl
chr6:166218540..166218614hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563820
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014098
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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