A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6112224



Internal ID22021459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:55586206..55586206hg38UCSC Ensembl
chr18:53253437..53253437hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17636891
Samples
Known GenesTCF4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6112224
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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