A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5638880



Internal ID21587185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:30213935..30213935hg38UCSC Ensembl
chr10:30502864..30502864hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38187
hg19187
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17070343
SamplesHG02492
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5638880
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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