A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6021288



Internal ID21930631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:21748346..21748438hg38UCSC Ensembl
chr18:19328307..19328399hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622018
Samples
Known GenesMIB1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6021288
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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