A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5637190



Internal ID21585495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:126358015..126358015hg38UCSC Ensembl
chr8:127370260..127370260hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17152780
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5637190
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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