A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2819343



Internal ID21264682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:67538297..67538625hg38UCSC Ensembl
chr9:65906803..65907123hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg38329
hg19321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv367n137
Supporting Variantsnssv13704355
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2819343
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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