A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018140



Internal ID19107357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:46859589..46924345hg38UCSC Ensembl
Innerchr8:47771211..47835967hg19UCSC Ensembl
Innerchr8:47890376..47955132hg18UCSC Ensembl
Cytoband8q11.1
Allele length
AssemblyAllele length
hg3864757
hg1964757
hg1864757
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7210n100
Supporting Variantsnssv3687454
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)nsv1018140
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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