A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17130265



Internal ID21415149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72510750..72518073hg38UCSC Ensembl
chr3:72559901..72567224hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg387324
hg197324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5574051
Supporting Variants
SamplesHG00514
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17130265
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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