A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17138316



Internal ID21497245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:47417894..47417894hg38UCSC Ensembl
chr3:47459384..47459384hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5610650
Supporting Variants
SamplesNA19238
Known GenesSCAP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17138316
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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