A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029330



Internal ID19118549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:43320424..43384640hg38UCSC Ensembl
Innerchr8:43175567..43239783hg19UCSC Ensembl
Innerchr8:43294724..43358940hg18UCSC Ensembl
Cytoband8p11.1
Allele length
AssemblyAllele length
hg3864217
hg1964217
hg1864217
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3687274
Samples
Known GenesPOTEA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029330
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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