A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978174



Internal ID12981556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1823914..1875372hg38UCSC Ensembl
Innerchr10:1866108..1917566hg19UCSC Ensembl
Innerchr10:1856108..1907566hg18UCSC Ensembl
Innerchr10:1856108..1907566hg17UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3851459
hg1951459
hg1851459
hg1751459
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34498
Supporting Variants
SamplesNA18974
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6978174
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