A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5629237



Internal ID21577542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101315776..101315776hg38UCSC Ensembl
chr8:102328004..102328004hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38381
hg19381
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17155198
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5629237
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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