A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7321n100



Internal ID22793408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:132795962..132844975hg38UCSC Ensembl
chr8:133808208..133857220hg19UCSC Ensembl
chr8:133877390..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 Variants
Supporting Variantsnsv1018288, nsv1029286, nsv1034810
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)dgv7321n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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