A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026714



Internal ID21936057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9583776..9583835hg38UCSC Ensembl
chr11:9605323..9605382hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17592532
Samples
Known GenesWEE1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026714
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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