A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6088049



Internal ID21997282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87914770..87914770hg38UCSC Ensembl
chr10:89674527..89674527hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17580890
Samples
Known GenesPTEN
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6088049
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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