A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5542937



Internal ID317292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74204936..74204936hg38UCSC Ensembl
chr15:74497277..74497277hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17701061
Samples
Known GenesSTRA6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5542937
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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