A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5639446



Internal ID21587751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:37719760..37719760hg38UCSC Ensembl
chr8:37577278..37577278hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17149751, nssv17155547
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5639446
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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