A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17126508



Internal ID21414419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:186433238..186433238hg38UCSC Ensembl
chr4:187354392..187354392hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38690
hg19690
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5640884
Supporting Variants
SamplesHG00513
Known GenesF11-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17126508
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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