A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563649



Internal ID336580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83944871..83944922hg38UCSC Ensembl
chr15:84613623..84613674hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg381306
hg191306
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17702612
Samples
Known GenesADAMTSL3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563649
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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