A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6089724



Internal ID21998957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:78310299..78310299hg38UCSC Ensembl
chr10:80070056..80070056hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38175
hg19175
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17582615
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6089724
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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