A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17628722



Internal ID21820769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:55586216..55586216hg38UCSC Ensembl
chr18:53253447..53253447hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38171
hg19171
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6105416
Supporting Variants
Samples
Known GenesTCF4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17628722
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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