A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14247718



Internal ID21306149
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 TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169619
Supporting Variants
SamplesNGO_25
Known GenesRXRA
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14247718
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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