A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6002082



Internal ID21911425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:41127401..41127525hg38UCSC Ensembl
chr8:40984920..40985044hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17593854
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6002082
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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