A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6343n100



Internal ID22792430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:47057928..47095453hg38UCSC Ensembl
chr7:47097526..47135051hg19UCSC Ensembl
chr7:47064051..47101576hg18UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg3837526
hg1937526
hg1837526
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1033805, nsv1020431, nsv1016441, nsv1021435
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)dgv6343n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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