A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5644129



Internal ID21592434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4149430..4149430hg38UCSC Ensembl
chr10:4191622..4191622hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17070251, nssv17070250
SamplesNA19239, HG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5644129
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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