A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17129033



Internal ID21504056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:58185663..58185726hg38UCSC Ensembl
chr3:58171390..58171453hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5582890
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17129033
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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