A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6105629



Internal ID22014862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:55296721..55296721hg38UCSC Ensembl
chr18:52963952..52963952hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17630341
Samples
Known GenesTCF4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6105629
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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