A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2819043



Internal ID21264381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113453340..113453555hg38UCSC Ensembl
chr9:116215620..116215835hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38216
hg19216
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv371n137
Supporting Variantsnssv13701663
Samples
Known GenesRGS3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2819043
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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