A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6563n100



Internal ID22792650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:110512818..110557355hg38UCSC Ensembl
chr7:110152875..110197412hg19UCSC Ensembl
chr7:109940111..109984648hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3844538
hg1944538
hg1844538
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1018254, nsv1028190, nsv1032748, nsv1022043, nsv1021693
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)dgv6563n100
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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