A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5543629



Internal ID317861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25847458..25847458hg38UCSC Ensembl
chr15:26092605..26092605hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17698588
Samples
Known GenesATP10A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5543629
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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