A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028951



Internal ID19118170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:43643874..43907538hg38UCSC Ensembl
Innerchr8:43499017..43762681hg19UCSC Ensembl
Innerchr8:43618174..43881838hg18UCSC Ensembl
Cytoband8p11.1
Allele length
AssemblyAllele length
hg38263665
hg19263665
hg18263665
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7194n100
Supporting Variantsnssv3687325
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)nsv1028951
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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