A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17148361



Internal ID21503831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3402417..3402417hg38UCSC Ensembl
chr6:3402651..3402651hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38269
hg19269
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5630921
Supporting Variants
SamplesNA19239
Known GenesSLC22A23
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17148361
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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