A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6805n100



Internal ID22792892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:1588960..1635474hg38UCSC Ensembl
chr8:1537126..1583640hg19UCSC Ensembl
chr8:1524533..1571047hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg3846515
hg1946515
hg1846515
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1026633, nsv1025125
Samples
Known GenesDLGAP2, LOC100507435
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6805n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss3
Observed Complex0
Frequencyn/a


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