A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6644n100



Internal ID22792731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140861022..140877135hg38UCSC Ensembl
chr7:140560822..140576935hg19UCSC Ensembl
chr7:140207291..140223404hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3816114
hg1916114
hg1816114
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1026995, nsv1017485
Samples
Known GenesBRAF
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6644n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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