A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5630735



Internal ID21579040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:63440213..63440213hg38UCSC Ensembl
chr8:64352771..64352771hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17152528, nssv17152981
SamplesHG03486, HG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5630735
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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