A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17125197



Internal ID21403070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:183336717..183336717hg38UCSC Ensembl
chr4:184257870..184257870hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38672
hg19672
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5627689
Supporting Variants
SamplesHG00171
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17125197
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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