A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17153005



Internal ID21457087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:69137406..69137406hg38UCSC Ensembl
chr5:68433233..68433233hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5625282
Supporting Variants
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17153005
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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