A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5562n100



Internal ID22791649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:7407089..7477796hg38UCSC Ensembl
chr5:7407202..7477909hg19UCSC Ensembl
chr5:7460202..7530909hg18UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3870708
hg1970708
hg1870708
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1025505, nsv1018700, nsv1015940, nsv1022891, nsv1024125, nsv1030545
Samples
Known GenesADCY2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5562n100
Frequency
Sample Size11257
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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