A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033328



Internal ID19122550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:17983025..18029905hg38UCSC Ensembl
Innerchr8:17840534..17887414hg19UCSC Ensembl
Innerchr8:17884814..17931694hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3846881
hg1946881
hg1846881
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7123n100
Supporting Variantsnssv3684185
Samples
Known GenesPCM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033328
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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