A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17093797



Internal ID21478421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:74482697..74482697hg38UCSC Ensembl
chr17:72478836..72478836hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5649041
Supporting Variants
SamplesHG03486
Known GenesCD300A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17093797
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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