A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6066353



Internal ID21975586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:31278832..31278832hg38UCSC Ensembl
chr8:31136348..31136348hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17572479
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6066353
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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