A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979281



Internal ID12633236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15670227..15728649hg38UCSC Ensembl
Innerchr19:15781037..15839459hg19UCSC Ensembl
Innerchr19:15642037..15700459hg18UCSC Ensembl
Innerchr19:15642037..15700459hg17UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3858423
hg1958423
hg1858423
hg1758423
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34230
Supporting Variants
SamplesNA18523
Known GenesCYP4F12, OR10H2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979281
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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