A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6072652



Internal ID21981885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:27080032..27080032hg38UCSC Ensembl
chr8:26937549..26937549hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576000
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6072652
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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