A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978511



Internal ID12982099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:59096142..59136505hg38UCSC Ensembl
Innerchr10:60855902..60896265hg19UCSC Ensembl
Innerchr10:60525908..60566271hg18UCSC Ensembl
Innerchr10:60525908..60566271hg17UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3840364
hg1940364
hg1840364
hg1740364
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34756
Supporting Variants
SamplesNA19129
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6978511
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