A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034989



Internal ID19124208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:36384499..36578726hg38UCSC Ensembl
Innerchr8:36242017..36436244hg19UCSC Ensembl
Innerchr8:36361575..36555402hg18UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38194228
hg19194228
hg18193828
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7160n100
Supporting Variantsnssv3685563
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)nsv1034989
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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