A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015709



Internal ID21925052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166162691..166162819hg38UCSC Ensembl
chr6:166576179..166576307hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17565689
Samples
Known GenesT
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015709
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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