A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6467n100



Internal ID20158083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73420075..73583448hg38UCSC Ensembl
chr7:72834405..72997778hg19UCSC Ensembl
chr7:72472341..72635714hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38163374
hg19163374
hg18163374
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1028905, nsv1023128
Samples
Known GenesBAZ1B, BCL7B, FZD9, TBL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6467n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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