A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6028212



Internal ID21937555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:85788520..85792853hg38UCSC Ensembl
chr11:85499563..85503896hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg384334
hg194334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584252
Samples
Known GenesSYTL2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6028212
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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