A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6008089



Internal ID21917432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:109317773..109317860hg38UCSC Ensembl
chr6:109638976..109639063hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17574515
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6008089
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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