A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032281



Internal ID19121503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:52328979..52470465hg38UCSC Ensembl
Innerchr8:53241539..53383025hg19UCSC Ensembl
Innerchr8:53404092..53545578hg18UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg38141487
hg19141487
hg18141487
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3687508
Samples
Known GenesST18
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032281
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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