A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028602



Internal ID19117820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:2308620..2725657hg38UCSC Ensembl
Innerchr8:2254675..2583198hg19UCSC Ensembl
Innerchr8:2242082..2570605hg18UCSC Ensembl
Cytoband8p23.2
Allele length
AssemblyAllele length
hg38417038
hg19328524
hg18328524
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6820n100
Supporting Variantsnssv3757804
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)nsv1028602
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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