A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6220n100



Internal ID20157836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:81400..231133hg38UCSC Ensembl
chr7:81400..231133hg19UCSC Ensembl
chr7:176483..326216hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38149734
hg19149734
hg18149734
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1018740, nsv1015739
Samples
Known GenesFAM20C, LOC100507642
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6220n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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