A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17065286



Internal ID21491200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:3433482..3433559hg38UCSC Ensembl
chr1:3350046..3350123hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5578625
Supporting Variants
SamplesNA19238
Known GenesPRDM16
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17065286
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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