A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6707n100



Internal ID22792794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:143549301..143773176hg38UCSC Ensembl
chr7:143246394..143470269hg19UCSC Ensembl
chr7:142956516..143101202hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38223876
hg19223876
hg18144687
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1023276, nsv1016415
Samples
Known GenesCTAGE15, CTAGE6, FAM115C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6707n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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