A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018288



Internal ID19107505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:132795962..132844975hg38UCSC Ensembl
Innerchr8:133808208..133857220hg19UCSC Ensembl
Innerchr8:133877390..133926402hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3849014
hg1949013
hg1849013
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7321n100
Supporting Variantsnssv3691571
Samples
Known GenesPHF20L1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018288
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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