A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6548n100



Internal ID20158164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107240508..107325770hg38UCSC Ensembl
chr7:106880953..106966215hg19UCSC Ensembl
chr7:106668189..106753451hg18UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3885263
hg1985263
hg1885263
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1016691, nsv1024903, nsv1015615, nsv1034707
Samples
Known GenesCOG5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6548n100
Frequency
Sample Size29084
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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