A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016614



Internal ID21925957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:48540921..48541416hg38UCSC Ensembl
chr8:49453481..49453976hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg38496
hg19496
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17590249
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016614
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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