A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6605n100



Internal ID20158221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:122924680..123134549hg38UCSC Ensembl
chr7:122564734..122774603hg19UCSC Ensembl
chr7:122351970..122561839hg18UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg38209870
hg19209870
hg18209870
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1027050, nsv1024170
Samples
Known GenesSLC13A1, TAS2R16
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6605n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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