A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169619



Internal ID21313430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:134429330..134519449hg38UCSC Ensembl
Outerchr9:134416396..134519971hg38UCSC Ensembl
Innerchr9:137321176..137411295hg19UCSC Ensembl
Outerchr9:137308242..137411817hg19UCSC Ensembl
Innerchr9:136460997..136551116hg18UCSC Ensembl
Outerchr9:136448063..136551638hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38103576
hg19103576
hg18103576
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14247718, nssv14244673
SamplesNGO_25, MLY_8
Known GenesRXRA
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169619
Frequency
Sample Size93
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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