A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2750886



Internal ID12984438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:19143845..19543165hg38UCSC Ensembl
Innerchr10:19432774..19832094hg19UCSC Ensembl
Innerchr10:19472780..19872100hg18UCSC Ensembl
Innerchr10:19472780..19872100hg17UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38399321
hg19399321
hg18399321
hg17399321
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv20e55
Supporting Variantsessv6989198, essv6987851, essv6980796, essv6980797, essv6980795
SamplesBEC_16
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Affymetrix Mapping 250K Sty2 SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv2750886
Frequency
Sample Size771
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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