A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3935843



Internal ID21355912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:69445378..69445691hg38UCSC Ensembl
chr8:70357613..70357926hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15198821
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3935843
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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