A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6589n100



Internal ID22792676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:112791348..112836701hg38UCSC Ensembl
chr7:112431403..112476756hg19UCSC Ensembl
chr7:112218639..112263992hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3845354
hg1945354
hg1845354
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1031405, nsv1023222
Samples
Known GenesC7orf60
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6589n100
Frequency
Sample Size11257
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer