A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3933029



Internal ID21353098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:138206341..138206341hg38UCSC Ensembl
chr8:139218584..139218584hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg381428
hg191428
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15204522
SamplesHG002
Known GenesFAM135B
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3933029
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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