A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988199



Internal ID12980402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:57815925..58007771hg38UCSC Ensembl
Innerchr10:59575685..59767531hg19UCSC Ensembl
Innerchr10:59245691..59437537hg18UCSC Ensembl
Innerchr10:59245691..59437537hg17UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38191847
hg19191847
hg18191847
hg17191847
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35063
Supporting Variants
SamplesNA18572
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6988199
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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