A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5631709



Internal ID21580014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:85447149..85447149hg38UCSC Ensembl
chr8:86359378..86359378hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17152146
SamplesNA19983
Known GenesCA3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5631709
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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