A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6061118



Internal ID21970351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:1799348..1799348hg38UCSC Ensembl
chr8:1747514..1747514hg19UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17572015
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6061118
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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