A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7121n100



Internal ID20158737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:17766079..17957752hg38UCSC Ensembl
chr8:17623588..17815261hg19UCSC Ensembl
chr8:17667868..17859541hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38191674
hg19191674
hg18191674
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1022749, nsv1023951
Samples
Known GenesFGL1, MTUS1, PCM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7121n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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