A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5543806



Internal ID318026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:51322579..51322579hg38UCSC Ensembl
chr15:51614776..51614776hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17702685
Samples
Known GenesCYP19A1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5543806
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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