A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5625065



Internal ID21573370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:54555423..54555423hg38UCSC Ensembl
chr8:55467983..55467983hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg38464
hg19464
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17155414
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5625065
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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