A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169673



Internal ID21313484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:37504706..37514035hg38UCSC Ensembl
Outerchr9:37502112..37515714hg38UCSC Ensembl
Innerchr9:37504703..37514032hg19UCSC Ensembl
Outerchr9:37502109..37515711hg19UCSC Ensembl
Innerchr9:37494703..37504032hg18UCSC Ensembl
Outerchr9:37492109..37505711hg18UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg3813603
hg1913603
hg1813603
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14243461, nssv14250416, nssv14243324, nssv14252156, nssv14250744, nssv14245280, nssv14244184
SamplesMLY_11, NGO_10, NGO_9, NGO_4, NGO_26, SNI_6, NGO_7
Known GenesFBXO10, POLR1E
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169673
Frequency
Sample Size93
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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