A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5534224



Internal ID214613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:81198745..81198745hg38UCSC Ensembl
chr15:81491086..81491086hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38995
hg19995
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17704001
Samples
Known GenesIL16
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5534224
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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