A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17129579



Internal ID21416217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:39053710..39053899hg38UCSC Ensembl
chr5:39053812..39054001hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg38190
hg19190
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5582364
Supporting Variants
SamplesHG00731
Known GenesRICTOR
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17129579
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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