A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3936412



Internal ID21356482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:142970296..142970296hg38UCSC Ensembl
chr8:144051713..144051713hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38237
hg19237
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15204161, nssv15204162
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3936412
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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