A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5644174



Internal ID21592479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103583767..103583767hg38UCSC Ensembl
chr10:105343524..105343524hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17068487
SamplesHG00731
Known GenesNEURL1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5644174
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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