A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17159273



Internal ID21493860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:54915508..54915835hg38UCSC Ensembl
chr6:54780306..54780633hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5572470
Supporting Variants
SamplesNA19238
Known GenesFAM83B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17159273
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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