A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031584



Internal ID19120806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:67630911..67644593hg38UCSC Ensembl
Innerchr8:68543146..68556828hg19UCSC Ensembl
Innerchr8:68705700..68719382hg18UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg3813683
hg1913683
hg1813683
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7236n100
Supporting Variantsnssv3689493, nssv3689494
Samples
Known GenesCPA6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031584
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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