A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17137344



Internal ID21414731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25845693..25845693hg38UCSC Ensembl
chr4:25847315..25847315hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5608867
Supporting Variants
SamplesHG00513
Known GenesSEL1L3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17137344
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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