A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17133892



Internal ID21459679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1123198..1123198hg38UCSC Ensembl
chr4:1116986..1116986hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5605575
Supporting Variants
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17133892
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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