A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6267n100



Internal ID22792354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:11672101..11734614hg38UCSC Ensembl
chr7:11711728..11774241hg19UCSC Ensembl
chr7:11678253..11740766hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3862514
hg1962514
hg1862514
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1035078, nsv1032001, nsv1026670
Samples
Known GenesTHSD7A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6267n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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