A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6471n100



Internal ID19016839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:76443262..76674181hg38UCSC Ensembl
chr7:76072579..76303498hg19UCSC Ensembl
chr7:75910515..76141434hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38230920
hg19230920
hg18230920
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1018487, nsv1019353, nsv1015799, nsv1015945
Samples
Known GenesDTX2, FDPSP2, LOC100133091, POMZP3, UPK3B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6471n100
Frequency
Sample Size29084
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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