A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6067912



Internal ID21977145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:105908503..105908503hg38UCSC Ensembl
chr8:106920731..106920731hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17593016
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6067912
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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