A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6009661



Internal ID21919004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:143030166..143030486hg38UCSC Ensembl
chr8:144111583..144111903hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17581676
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6009661
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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