A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6062380



Internal ID21971613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38561067..38561067hg38UCSC Ensembl
chr8:38418585..38418585hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17568087
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6062380
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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