A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6252n100



Internal ID22792339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:7476493..7562007hg38UCSC Ensembl
chr7:7516124..7601638hg19UCSC Ensembl
chr7:7482649..7568163hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3885515
hg1985515
hg1885515
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1024107, nsv1027872
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)dgv6252n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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