A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17703168



Internal ID126834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60517485..60517514hg38UCSC Ensembl
chr15:60809684..60809713hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5546968
Supporting Variants
Samples
Known GenesRORA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17703168
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.042616


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