A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3942768



Internal ID21362837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:121143037..121143037hg38UCSC Ensembl
chr8:122155277..122155277hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15204968
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3942768
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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