A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17121387



Internal ID21477205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:158501902..158501957hg38UCSC Ensembl
chr5:157928910..157928965hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5583420
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17121387
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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