A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6024581



Internal ID21933924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:17830606..17830683hg38UCSC Ensembl
chr11:17852153..17852230hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584351
Samples
Known GenesSERGEF
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6024581
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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