A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018697



Internal ID19107914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:90715646..90774759hg38UCSC Ensembl
Innerchr8:91727874..91786987hg19UCSC Ensembl
Innerchr8:91797050..91856163hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3859114
hg1959114
hg1859114
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689706
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)nsv1018697
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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