A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6060932



Internal ID21970165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:89994290..89994290hg38UCSC Ensembl
chr8:91006518..91006518hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17577720
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6060932
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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