A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6024102



Internal ID21933445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:4039355..4039485hg38UCSC Ensembl
chr11:4060585..4060715hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17582423
Samples
Known GenesSTIM1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6024102
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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