A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7320n100



Internal ID22793407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:132783362..132860065hg38UCSC Ensembl
chr8:133795608..133872310hg19UCSC Ensembl
chr8:133864790..133941492hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3876704
hg1976703
hg1876703
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1015942, nsv1015502, nsv1016843, nsv1030953, nsv1018211, nsv1030014, nsv1034433, nsv1031473, nsv1028551
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)dgv7320n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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