A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17137091



Internal ID21438605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:190237619..190237919hg38UCSC Ensembl
chr3:189955408..189955708hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5569837
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17137091
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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