A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3925699



Internal ID21345773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66376332..66376332hg38UCSC Ensembl
chr8:67288567..67288567hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15204917
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3925699
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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