A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6010120



Internal ID21919463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97334295..97334364hg38UCSC Ensembl
chr10:99094052..99094121hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17582931
Samples
Known GenesFRAT2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6010120
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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