A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5427316



Internal ID206222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74543611..74543662hg38UCSC Ensembl
chr15:74835952..74836003hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17701080
Samples
Known GenesARID3B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5427316
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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