A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5632029



Internal ID21580334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:130535525..130535525hg38UCSC Ensembl
chr8:131547771..131547771hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38346
hg19346
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17157984
SamplesHG02492
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5632029
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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