A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6615n100



Internal ID20158231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:128287910..128308551hg38UCSC Ensembl
chr7:127927963..127948604hg19UCSC Ensembl
chr7:127715199..127735840hg18UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg3820642
hg1920642
hg1820642
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1016669, nsv1018630, nsv1019036, nsv1017782
Samples
Known GenesMGC27345
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6615n100
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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