A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6109044



Internal ID22018277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:13675231..13675231hg38UCSC Ensembl
chr18:13675230..13675230hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622179
Samples
Known GenesFAM210A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6109044
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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