A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4674n100



Internal ID20156290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:6680357..7004828hg38UCSC Ensembl
chr3:6722044..7046515hg19UCSC Ensembl
chr3:6697044..7021515hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38324472
hg19324472
hg18324472
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1000670, nsv1005826
Samples
Known GenesGRM7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4674n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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