A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17138077



Internal ID21475930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:25938372..25941018hg38UCSC Ensembl
chr5:25938481..25941127hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg382647
hg192647
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5579933
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17138077
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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