A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3945039



Internal ID21365108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:133757818..133757867hg38UCSC Ensembl
chr8:134770061..134770110hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15198894
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3945039
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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