A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17082914



Internal ID21468100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:35080740..35080793hg38UCSC Ensembl
chr15:35372941..35372994hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5599806
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17082914
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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