A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024285



Internal ID19113502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:101375798..101390702hg38UCSC Ensembl
Innerchr8:102388026..102402930hg19UCSC Ensembl
Innerchr8:102457202..102472106hg18UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3814905
hg1914905
hg1814905
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7277n100
Supporting Variantsnssv3691244, nssv3691247, nssv3691246, nssv3691240, nssv3691237, nssv3691235, nssv3691236, nssv3689756, nssv3691245, nssv3691243, nssv3691241, nssv3691233, nssv3691234, nssv3691238, nssv3691239, nssv3691242
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024285
Frequency
Sample Size11257
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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