A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6144807



Internal ID344012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:10642000..10648000hg38UCSC Ensembl
chr18:10641997..10647997hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg386001
hg196001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17715378
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6144807
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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