A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6080501



Internal ID21989734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:29938900..29938900hg38UCSC Ensembl
chr10:30227829..30227829hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17583122
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6080501
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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