A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6022129



Internal ID21931472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9923281..9923376hg38UCSC Ensembl
chr18:9923278..9923373hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17626194
Samples
Known GenesVAPA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6022129
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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