A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3952065



Internal ID21372134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:88014562..88014640hg38UCSC Ensembl
chr8:89026790..89026868hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15199591
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3952065
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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