A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17704170



Internal ID127836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90083143..90235813hg38UCSC Ensembl
chr15:90626375..90779045hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38152671
hg19152671
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6144385
Supporting Variants
Samples
Known GenesCIB1, GDPGP1, IDH2, SEMA4B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17704170
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000781


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