A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6038186



Internal ID21947529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65388181..65388803hg38UCSC Ensembl
chr11:65155652..65156274hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38623
hg19623
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17594012
Samples
Known GenesFRMD8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6038186
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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