A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169485



Internal ID21313968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5385783..5398011hg38UCSC Ensembl
Outerchr9:5384069..5405540hg38UCSC Ensembl
Innerchr9:5385783..5398011hg19UCSC Ensembl
Outerchr9:5384069..5405540hg19UCSC Ensembl
Innerchr9:5375783..5388011hg18UCSC Ensembl
Outerchr9:5374069..5395540hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3821472
hg1921472
hg1821472
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14248236
SamplesNGO_1
Known GenesPLGRKT
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169485
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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