A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170218



Internal ID21314279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:85088630..85149161hg38UCSC Ensembl
Outerchr9:85085616..85151361hg38UCSC Ensembl
Innerchr9:87703545..87764076hg19UCSC Ensembl
Outerchr9:87700531..87766276hg19UCSC Ensembl
Innerchr9:86893365..86953896hg18UCSC Ensembl
Outerchr9:86890351..86956096hg18UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3865746
hg1965746
hg1865746
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14252239, nssv14252147
SamplesNGO_27, NGO_36
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170218
Frequency
Sample Size93
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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