A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17703898



Internal ID127564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68286870..68286922hg38UCSC Ensembl
chr15:68579208..68579260hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6145042
Supporting Variants
Samples
Known GenesFEM1B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17703898
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.011282


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