A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5629145



Internal ID21577450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42182378..42182378hg38UCSC Ensembl
chr8:42039896..42039896hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17149916
SamplesHG00731
Known GenesPLAT
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5629145
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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