A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5615029



Internal ID21563334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:18861554..18861554hg38UCSC Ensembl
chr4:18863177..18863177hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17129756
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5615029
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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