A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3687453



Internal ID18985734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:46847115..46929159hg38UCSC Ensembl
Innerchr8:47758737..47840781hg19UCSC Ensembl
Innerchr8:47877902..47959946hg18UCSC Ensembl
Cytoband8q11.1
Allele length
AssemblyAllele length
hg3882045
hg1982045
hg1882045
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033221
Supporting Variants
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)nssv3687453
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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