A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028892



Internal ID19118111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:45935900..46992815hg38UCSC Ensembl
Innerchr8:46847522..47904438hg19UCSC Ensembl
Innerchr8:46966687..48023603hg18UCSC Ensembl
Cytoband8q11.1
Allele length
AssemblyAllele length
hg381056916
hg191056917
hg181056917
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7203n100
Supporting Variantsnssv3687393
Samples
Known GenesLINC00293
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028892
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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