A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17705245



Internal ID128911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:98854051..99246003hg38UCSC Ensembl
chr15:99397280..99786208hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38391953
hg19388929
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5521512
Supporting Variants
Samples
Known GenesIGF1R, PGPEP1L, SYNM, TTC23
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17705245
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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