A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6076455



Internal ID21985688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:13016235..13016235hg38UCSC Ensembl
chr8:12873744..12873744hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17572147
Samples
Known GenesKIAA1456
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6076455
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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