A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6604n100



Internal ID22792691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:122203647..122293112hg38UCSC Ensembl
chr7:121843701..121933166hg19UCSC Ensembl
chr7:121630937..121720402hg18UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg3889466
hg1989466
hg1889466
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1034945, nsv1024364, nsv1020645
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)dgv6604n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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