A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5634155



Internal ID21582460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:48148237..48148237hg38UCSC Ensembl
chr8:49060797..49060797hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg38645
hg19645
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17139867
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5634155
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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