A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6021309



Internal ID21930652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62563067..62564421hg38UCSC Ensembl
chr11:62330539..62331893hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg381355
hg191355
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585708
Samples
Known GenesEEF1G
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6021309
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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