A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028633



Internal ID19117851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:2473547..2725119hg38UCSC Ensembl
Innerchr8:2330755..2582660hg19UCSC Ensembl
Innerchr8:2318162..2570067hg18UCSC Ensembl
Cytoband8p23.2
Allele length
AssemblyAllele length
hg38251573
hg19251906
hg18251906
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6820n100
Supporting Variantsnssv3757810, nssv3675249, nssv3675247, nssv3675246, nssv3675245, nssv3675251, nssv3675250, nssv3675248
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)nsv1028633
Frequency
Sample Size11257
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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