A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5642178



Internal ID21590483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:154951529..154951529hg38UCSC Ensembl
chr6:155272663..155272663hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg38204
hg19204
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17141694
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5642178
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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