A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17125705



Internal ID21402354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:18084798..18086329hg38UCSC Ensembl
chr5:18084907..18086438hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg381532
hg191532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5568742
Supporting Variants
SamplesHG00171
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17125705
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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