A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17130870



Internal ID21492670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:124630676..124630676hg38UCSC Ensembl
chr4:125551831..125551831hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5608526
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17130870
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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