A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6146124



Internal ID345329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:46702717..46830267hg38UCSC Ensembl
chr18:44282680..44410230hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg38127551
hg19127551
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17717913
Samples
Known GenesPIAS2, ST8SIA5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6146124
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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