A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6550n100



Internal ID22792637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:109759022..109818869hg38UCSC Ensembl
chr7:109399079..109458926hg19UCSC Ensembl
chr7:109186315..109246162hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3859848
hg1959848
hg1859848
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1021772, nsv1023020, nsv1024619, nsv1021654, nsv1020873, nsv1015974, nsv1027222
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6550n100
Frequency
Sample Size11257
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


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