A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17135553



Internal ID21417020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39468792..39469083hg38UCSC Ensembl
chr3:39510283..39510574hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38292
hg19292
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5564850
Supporting Variants
SamplesHG00731
Known GenesMOBP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17135553
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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