A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028273



Internal ID19117491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:45935900..46151810hg38UCSC Ensembl
Innerchr8:46847522..47063432hg19UCSC Ensembl
Innerchr8:46966687..47182597hg18UCSC Ensembl
Cytoband8q11.1
Allele length
AssemblyAllele length
hg38215911
hg19215911
hg18215911
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7200n100
Supporting Variantsnssv3687372, nssv3687373
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)nsv1028273
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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