A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026428



Internal ID21935771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:55586153..55586204hg38UCSC Ensembl
chr18:53253384..53253435hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17632247
Samples
Known GenesTCF4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026428
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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