A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13704287



Internal ID21226092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113453340..113453531hg38UCSC Ensembl
chr9:116215620..116215811hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38192
hg19192
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2819069
Supporting Variants
Samples
Known GenesRGS3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13704287
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.984375


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