A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027246



Internal ID19116465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:9995202..10024966hg38UCSC Ensembl
Innerchr8:9852712..9882476hg19UCSC Ensembl
Innerchr8:9890122..9919886hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3829765
hg1929765
hg1829765
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3681711
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)nsv1027246
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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