A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033234



Internal ID18775768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:21915873..21974708hg38UCSC Ensembl
Innerchr8:21773384..21832219hg19UCSC Ensembl
Innerchr8:21829330..21888165hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3858836
hg1958836
hg1858836
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7131n100
Supporting Variantsnssv3685353
Samples
Known GenesXPO7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033234
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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