A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3929408



Internal ID21349478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:75383647..75383737hg38UCSC Ensembl
chr9:77998563..77998653hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15199250
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3929408
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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