A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029808



Internal ID21939151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:21592381..21592434hg38UCSC Ensembl
chr18:19172342..19172395hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17636392
Samples
Known GenesESCO1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029808
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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