A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17131990



Internal ID21423747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:83501809..83501809hg38UCSC Ensembl
chr4:84422962..84422962hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5608863
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17131990
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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