A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17703787



Internal ID127453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:99731565..99947520hg38UCSC Ensembl
chr15:100271770..100487725hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38215956
hg19215956
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560242
Supporting Variants
Samples
Known GenesDNM1P46, LYSMD4
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17703787
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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