A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5882226



Internal ID22657203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:55590089..55592090hg38UCSC Ensembl
chr18:53257320..53259321hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg382002
hg192002
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17471366
Samples
Known GenesTCF4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5882226
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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