A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6203n100



Internal ID20157819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168843444..169398234hg38UCSC Ensembl
chr6:169243539..169798329hg19UCSC Ensembl
chr6:168985464..169540254hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38554791
hg19554791
hg18554791
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1018282, nsv1032812
Samples
Known GenesTHBS2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6203n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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