A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5634786



Internal ID21583091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:51111163..51111163hg38UCSC Ensembl
chr5:50406997..50406997hg19UCSC Ensembl
Cytoband5q11.1
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17131573
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5634786
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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