A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6009342



Internal ID21918685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:83510310..83510434hg38UCSC Ensembl
chr8:84422545..84422669hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17583792
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6009342
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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