A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6290n100



Internal ID20157906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:16874165..17376469hg38UCSC Ensembl
chr7:16913789..17416093hg19UCSC Ensembl
chr7:16880314..17382618hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38502305
hg19502305
hg18502305
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1019491, nsv1023794, nsv1028248
Samples
Known GenesAGR3, AHR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6290n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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