A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6614n100



Internal ID22792701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:126403590..126427352hg38UCSC Ensembl
chr7:126043644..126067406hg19UCSC Ensembl
chr7:125830880..125854642hg18UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg3823763
hg1923763
hg1823763
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1025757, nsv1030866, nsv1023102, nsv1018179, nsv1020879
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6614n100
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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