A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014276



Internal ID21923619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:105847561..105847625hg38UCSC Ensembl
chr6:106295436..106295500hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17564388
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014276
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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