A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6076273



Internal ID21985506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:53468900..53468900hg38UCSC Ensembl
chr8:54381460..54381460hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17583171
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6076273
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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