A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3951255



Internal ID21371324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121092516..121092683hg38UCSC Ensembl
chr9:123854794..123854961hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15198999
SamplesHG002
Known GenesCNTRL
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3951255
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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