A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019676



Internal ID21929019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:127740093..127740144hg38UCSC Ensembl
chr10:129538357..129538408hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584569
Samples
Known GenesFOXI2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019676
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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