A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6251n100



Internal ID22792338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:7285169..7389929hg38UCSC Ensembl
chr7:7324800..7429560hg19UCSC Ensembl
chr7:7291325..7396085hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38104761
hg19104761
hg18104761
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1026321, nsv1015977, nsv1016422, nsv1015201
Samples
Known GenesCOL28A1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6251n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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