A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028650



Internal ID19117868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:10244305..10321027hg38UCSC Ensembl
Innerchr8:10101815..10178537hg19UCSC Ensembl
Innerchr8:10139225..10215947hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3876723
hg1976723
hg1876723
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3681715
Samples
Known GenesMSRA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028650
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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