A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5657134



Internal ID21605439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:2172929..2172929hg38UCSC Ensembl
chr20:2153575..2153575hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17116474
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5657134
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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