A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2819453



Internal ID21264791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128464667..128464862hg38UCSC Ensembl
chr9:131226946..131227141hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13705221
Samples
Known GenesODF2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2819453
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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