A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5452975



Internal ID231116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:14415314..14415419hg38UCSC Ensembl
chr3:14456822..14456927hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16930152
Samples
Known GenesSLC6A6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5452975
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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