A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6056777



Internal ID21966011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:25578219..25578291hg38UCSC Ensembl
chr20:25558855..25558927hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17636127
Samples
Known GenesNINL
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6056777
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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