A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6078777



Internal ID21988010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30665021..30665021hg38UCSC Ensembl
chr8:30522538..30522538hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17577113
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6078777
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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