A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5525764



Internal ID301912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100327429..100440846hg38UCSC Ensembl
chr15:100867634..100981051hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38113418
hg19113418
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17703840
Samples
Known GenesADAMTS17, CERS3, SPATA41
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5525764
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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