A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5625953



Internal ID21574258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:64686201..64686201hg38UCSC Ensembl
chr8:65598758..65598758hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17144476
SamplesHG03065
Known GenesCYP7B1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5625953
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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