A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015702



Internal ID19104920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:42290622..42301240hg38UCSC Ensembl
Innerchr8:42148140..42158758hg19UCSC Ensembl
Innerchr8:42267297..42277915hg18UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3810619
hg1910619
hg1810619
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7185n100
Supporting Variantsnssv3687263
Samples
Known GenesIKBKB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015702
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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