A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016224



Internal ID18758759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:52807381..53454974hg38UCSC Ensembl
Innerchr8:53719941..54367534hg19UCSC Ensembl
Innerchr8:53882494..54530087hg18UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg38647594
hg19647594
hg18647594
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3687520
Samples
Known GenesNPBWR1, OPRK1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016224
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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